Production system/production process for acrylic acid and precursors thereof

ABSTRACT

Provided herein are systems, and methods of using such systems, for producing acrylic acid from ethylene oxide and carbon monoxide on an industrial scale. The composition includes: polypropiolactone having a concentration of greater than at least 90 wt %; a residual cobalt or ions thereof from a carbonylation catalyst in an amount of 10 ppm or less; acetic acid in an amount of 10 ppm or less; and tetrahydrofuran in amount of 10 ppm or less.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of and claims benefit fromU.S. Ser. No. 16/739,733, filed on Jul. 10, 2020 and is a divisional ofand claims benefit from U.S. Ser. No. 15/223,178 filed Jul. 29, 2016,which claims the benefit of U.S. Provisional Ser. No. 62/199,918 filedJul. 31, 2015, which are hereby incorporated by reference in itsentirety as if fully restated herein.

FIELD

The present disclosure relates generally to systems and methods forproducing acrylic acid and precursors thereof, including β-propiolactoneand polypropiolactone, from ethylene oxide and carbon monoxide.

BACKGROUND

Polypropiolactone is a biodegradable polymer that can be used in manypackaging and thermoplastic applications. Polypropiolactone is also auseful precursor for the production of acrylic acid. Polypropiolactonemay serve as a precursor for glacial acrylic acid, which is in highdemand for the production of polyacrylic acid-based superabsorbentpolymers, detergent co-builders, dispersants, flocculants andthickeners. One advantage of polypropiolactone is that it can be safelytransported and stored for extended periods of time without the safetyor quality concerns associated with shipping and storing glacial acrylicacid. There additionally is interest in glacial acrylic acid which canbe produced from biomass-derived feedstock, petroleum-derived feedstock,or combinations thereof. Given the size of the acrylic acid market andthe importance of downstream applications of acrylic acid, there is aneed for industrial systems and methods to produce acrylic acid andprecursors thereof.

BRIEF SUMMARY

Provided herein are systems and processes for the production of acrylicacid and precursors thereof, including β-propiolactone andpolypropiolactone, and methods of using such productionsystem/production process. In some aspects, provided is a productionsystem/production process and a production process for glacial acrylicacid from ethylene oxide and carbon monoxide that includes aβ-propiolactone production system/production process, a carbonylationcatalyst recycling apparatus, a β-propiolactone purification system, apolypropiolactone production system/production process, and a glacialacrylic acid production system/production process.

In some embodiments, the β-propiolactone production system/productionprocess includes a carbon monoxide source, an ethylene oxide source, acarbonylation catalyst source, a solvent source, and a carbonylationreactor. In certain variations, the carbonylation reactor has at leastone inlet to receive carbon monoxide from the carbon monoxide source,ethylene oxide from the ethylene oxide source, carbonylation catalystfrom the carbonylation catalyst source, and solvent from the solventsource; and an outlet to output a first β-propiolactone stream, whereinthe first β-propiolactone stream comprises β-propiolactone, solvent,ethylene oxide, carbonylation catalyst, acetaldehyde, and succinicanhydride.

In some embodiments, the carbonylation catalyst recycling apparatus isconfigured to separate at least a portion of the catalyst from the firstβ-propiolactone stream and produce a recycle catalyst stream and asecond β-propiolactone stream. In some variations, the recycle catalyststream includes separated carbonylation catalyst. In some variations,the second β-propiolactone stream includes β-propiolactone, solvent,ethylene oxide, catalyst, acetaldehyde, and succinic anhydride. In otherembodiments, the carbonylation catalyst recycling apparatus has an inletto receive the first β-propiolactone stream from the β-propiolactoneproduction system/production process; a recycle outlet to output therecycle catalyst stream to the carbonylation reactor; and aβ-propiolactone outlet to output the second β-propiolactone stream.

In other embodiments, the β-propiolactone purification system includesan evaporator, a stripper, and a vacuum column. In some variations, theevaporator is configured to receive the second β-propiolactone streamfrom the carbonylation catalyst recycling apparatus, and separate thesecond β-propiolactone stream into: a first overhead stream thatincludes (i) at least 75 wt % of solvent, (ii) less than 20 wt % ofβ-propiolactone, and (iii) less than 5 wt % of ethylene oxide andacetaldehyde, and a first bottoms stream that includes: (i) at least 75wt % of β-propiolactone, (ii) less than 20 wt % of solvent, and (iii)less than 5 wt % of catalyst, acetaldehyde, and succinic anhydride.

In some variations, the stripper is configured to receive the firstoverhead stream from the evaporator, and separate the first overheadstream into: a second overhead stream that includes (i) at least 25 wt %of ethylene oxide and acetaldehyde, and (ii) less than 75 wt % ofsolvent, a side stream comprising solvent, and a second bottoms streamcomprising β-propiolactone.

In some variations, the vacuum column is configured to receive the firstbottoms stream from the evaporator, and the second bottoms stream fromthe stripper and mix the first bottoms stream and the second bottomsstream to produce a mixed bottoms stream, separate the first bottomsstream and second bottoms stream into: a third overhead streamcomprising solvent, and a third bottoms stream comprisingβ-propiolactone.

In some embodiments, the polypropiolactone production system/productionprocess includes: a polymerization initiator or catalyst source; atleast one polymerization reactor to receive the third bottoms streamfrom the β-propiolactone purification system and the polymerizationinitiator or catalyst from the polymerization initiator or catalystsource, and to output a polypropiolactone stream, wherein thepolypropiolactone stream comprises polypropiolactone andβ-propiolactone.

In other embodiments, the glacial acrylic acid productionsystem/production process includes a thermolysis reactor, which has aninlet to receive the polypropiolactone stream from the polypropiolactoneproduction system/production process, and an outlet to output a glacialacrylic acid stream, wherein the glacial acrylic acid stream comprisesglacial acrylic acid.

In other aspects, provided is a polypropiolactone productionsystem/production process that includes: a β-propiolactone source; apolymerization initiator or catalyst source; a first polymerizationreactor; and a second polymerization reactor.

In some variations, the first polymerization reactor includes: aβ-propiolactone inlet to receive β-propiolactone from theβ-propiolactone source; a first catalyst inlet to receive catalyst fromthe polymerization catalyst source; and a first mixture outlet to outputa first mixture. In one variation, the first mixture comprisespolypropiolactone, β-propiolactone, and polymerization catalyst.

In other variations, the second polymerization reactor positioned afterthe first polymerization reactor, and includes: a mixture inlet toreceive the first mixture from the first polymerization reactor; asecond catalyst inlet to receive additional polymerization catalyst fromthe carbonylation catalyst source; and a second mixture outlet to outputa second mixture. In one variation, the second mixture comprisespolypropiolactone, β-propiolactone, and polymerization catalyst.

In certain aspects, provided is a β-propiolactone polymerizer thatincludes: a mixing zone configured to mix β-propiolactone and acatalyst; and a plurality of cooling zones positioned after the mixingzone. In some variations, the β-propiolactone polymerizer has a reactionlength. In certain variations, up to 95% of the β-propiolactone ispolymerized in the presence of the initiator or catalyst to formpolypropiolactone in the first 25% of the reaction length.

In other aspects, provided is a method for continuously producingpolypropiolactone, that includes: continuously feeding β-propiolactoneinto a first reactor; continuously feeding catalyst into the firstreactor; producing a first mixture comprising polypropiolactone,unreacted β-propiolactone, and residual catalyst in the first reactor,transferring the first mixture from the first reactor to a secondreactor; feeding additional catalyst from the catalyst source to thesecond reactor; producing a second mixture comprising polypropiolactone,unreacted β-propiolactone, and residual catalyst in the second reactor.

In some variations of the method, the first reactor has: aβ-propiolactone inlet to receive the β-propiolactone from aβ-propiolactone source; a first catalyst inlet to receive the catalystfrom a catalyst source; and a first mixture outlet to output the firstmixture. In other variations of the method, the second reactor has: amixture inlet to receive the first mixture from the first reactor; asecond catalyst inlet to receive the additional catalyst from thecatalyst source; and a second mixture outlet to output the secondmixture.

In yet other aspects, provided is a polypropiolactone productionsystem/production process that includes: a β-propiolactone source; afirst reactor; and a second reactor. In some embodiments, the firstreactor has: a β-propiolactone inlet to receive β-propiolactone from theβ-propiolactone source, a bed of supported catalyst or supportedcatalyst precursor, and a first mixture outlet to output a firstmixture. In one variation, the first mixture comprises polypropiolactoneand unreacted β-propiolactone. In other embodiments, the second reactoris positioned after the first reactor. In some variations, the mixtureinlet is configured to receive the first mixture from the first reactor,a second bed of supported catalyst or supported catalyst precursor, anda second mixture outlet to output a second mixture. In one variation,the second mixture comprises polypropiolactone and unreactedβ-propiolactone.

In yet other aspects, provided is a solid transportable polymercomposition that includes: at least 95 wt % of β-propiolactone; lessthan 10 ppm of cobalt or ions thereof; less than 10 ppm of aluminum orions thereof; less than 10 ppm acetic acid; and less than 10 ppm oftetrahydrofuran.

In another aspect, provided is a β-propiolactone purification systemthat includes: an evaporator; a first column, and a second column. Insome embodiments, the evaporator configured to receive a feed stream,wherein the feed stream comprises β-propiolactone, solvent, and separatethe feed stream into: a first overhead stream comprising: (i) at least75 wt % solvent, and (ii) at most 20 wt % β-propiolactone; and a firstbottoms stream comprising: (i) at least 75 wt % β-propiolactone, and(ii) at most 20 wt % solvent.

In some variations, the first column is configured to receive the firstoverhead stream from the evaporator, and separate the first overheadstream into: a second overhead stream comprising: (i) at least 35 wt %ethylene oxide, and (ii) at most 60 wt % solvent; a side streamcomprising solvent; and a second bottoms stream comprising at least 75wt % β-propiolactone.

In other variations, the second column is configured to receive thefirst bottoms stream from the evaporator, and the second bottoms streamfrom the first column, and separate the first bottoms stream and secondbottoms stream into: a third overhead stream comprising at least 95 wt %solvent; and a third bottoms stream comprising at least 95 wt %β-propiolactone.

In one aspect, provided is a β-propiolactone composition that includesat least 95 wt % of β-propiolactone; less than 10 ppm of cobalt or ionsthereof; less than 10 ppm of aluminum or ions thereof; less than 10 ppmacetic acid; and less than 10 ppm of tetrahydrofuran.

In yet other aspects, provided is a β-propiolactone productionsystem/production process that includes: a carbon monoxide source; anethylene oxide source; a carbonylation catalyst source; a solventsource; a recycled solvent storage tank; a reactor; and a purificationapparatus. In some embodiments, the reactor has: at least one inlet toreceive carbon monoxide from the carbon monoxide source, ethylene oxidefrom the ethylene oxide source, carbonylation catalyst from thecarbonylation catalyst source, and solvent from the solvent source andthe recycled solvent storage tank; and an outlet to output a mixture,wherein the mixture comprises β-propiolactone, solvent, unreacted carbonmonoxide, unreacted ethylene oxide, and carbonylation catalyst. In otherembodiments, the purification apparatus is configured to: separatesolvent from the mixture, and transfer the separated solvent to therecycled solvent reservoir.

In one aspect, provided is a glacial acrylic acid productionsystem/production process that includes: a polypropiolactone source; anda reactor. In some embodiments, the polypropiolactone source includes:at least 95 wt % of polypropiolactone; less than 10 ppm of cobalt orions thereof; less than 10 ppm of aluminum or ions thereof; less than 10ppm acetic acid; and less than 10 ppm of tetrahydrofuran. In otherembodiments, the reactor has: an inlet configured to receive thepolypropiolactone from the polypropiolactone source; and an outletconfigured to output a mixture, wherein the mixture comprises glacialacrylic acid.

In yet other aspects, provided is a separation system that includes: afeed source; a membrane; a first pump; and a second pump. In someembodiments, the membrane has: an inlet to receive a feed stream fromthe feed source, wherein the feed stream comprises β-propiolactone,catalyst and solvent; a catalyst outlet to output a catalyst recyclingstream comprising catalyst and solvent; and a β-propiolactone outlet tooutput a β-propiolactone stream comprising β-propiolactone and solvent.In other embodiments, the first pump is configured to pump the feedstream from the feed source to the membrane. In yet other embodiments,the second pump is configured to pump the catalyst recycling stream to aβ-propiolactone production system/production process.

The present teachings provide: a composition comprising:polypropiolactone having a concentration of greater than at least 90 wt%; a residual cobalt or ions thereof from a carbonylation catalyst in anamount of 10 ppm or less; acetic acid in an amount of 10 ppm or less;and tetrahydrofuran in amount of 10 ppm or less.

The present teachings provide: a composition comprising:polypropiolactone having a concentration of greater than at least 95 wt%; a residual cobalt or ions thereof from a carbonylation catalyst in anamount of 10 ppm or less; aluminum in an amount of 10 ppm or less; andtetrahydrofuran in amount of 10 ppm or less.

DESCRIPTION OF THE FIGURES

The present application can be best understood by reference to thefollowing description taken in conjunction with the accompanyingfigures, in which like parts may be referred to by like numerals.

FIG. 1 is a schematic illustration of a system to produce acrylic acidfrom carbon monoxide and ethylene oxide.

FIG. 2 is a schematic illustration of the unit operations to producepolypropiolactone from β-propiolactone, and glacial acrylic acid frompolypropiolactone.

FIG. 3 is a schematic illustration of a carbonylation catalyst recyclesystem that employs membranes, configured to isolate residualcarbonylation catalyst from a β-propiolactone product stream.

FIG. 4A is a schematic illustration of a system for convertingβ-propiolactone to polypropiolactone that involves the use of twocontinuous stirred-tank reactors in series.

FIG. 4B is a schematic illustration of a system for convertingβ-propiolactone to polypropiolactone that involves the use of two loopreactors in series.

FIG. 5 is a schematic illustration of a system for convertingβ-propiolactone to polypropiolactone that involves a plug flow reactorwith multiple cooling zones.

FIGS. 6, 7, 8, 9, 10, 11, 12, and 13 depict various configurations ofproduction system/production processes to produce glacial acrylic acidfrom ethylene oxide and carbon monoxide, via the production ofβ-propiolactone and polypropiolactone.

FIG. 14 illustrates an embodiment of an acrylic acid productionsystem/production process described herein.

FIG. 15 illustrates an embodiment of a carbonylation reaction systemdescribed herein.

FIG. 16 illustrates an embodiment of a BPL purification system describedherein.

FIGS. 17, 18, 19, and 20 are plots associated with Example 1 and show aplot of PPL and bPL peak absorbances as a function of time; an ¹H NMR ofthe isolated solid; a TGA of the isolated solid; and Melt rheology dataof the isolated solid at 120° C.

FIGS. 21, 22, 23, and 24 are plots associated with Example 2 and show aplot of PPL and bPL peak absorbances as a function of time; an ¹H NMR ofthe isolated solid; a TGA of the isolated solid; and Melt rheology dataof the isolated solid at 120° C.

FIGS. 25, 26, 27, and 28 are plots associated with Example 4 and show ¹HNMR plots indicating recovery of acrylic acid.

FIG. 29 are plots associated with Example 5 and shows an ¹H NMR plotindicating recovery of acrylic acid.

DETAILED DESCRIPTION

The following description sets forth exemplary methods, parameters andthe like. It should be recognized, however, that such description is notintended as a limitation on the scope of the present disclosure but isinstead provided as a description of exemplary embodiments.

Definitions

Definitions of specific functional groups and chemical terms aredescribed in more detail below. The chemical elements are identified inaccordance with the Periodic Table of the Elements, CAS version,Handbook of Chemistry and Physics, 75^(th) Ed., inside cover, andspecific functional groups are generally defined as described therein.Additionally, general principles of organic chemistry, as well asspecific functional moieties and reactivity, are described in OrganicChemistry, Thomas Sorrell, University Science Books, Sausalito, 1999;Smith and March March's Advanced Organic Chemistry, 5th Edition, JohnWiley & Sons, Inc., New York, 2001; Larock, Comprehensive OrganicTransformations, VCH Publishers, Inc., New York, 1989; Carruthers, SomeModern Methods of Organic Synthesis, 3^(rd) Edition, CambridgeUniversity Press, Cambridge, 1987; the entire contents of each of whichare incorporated herein by reference.

The terms “halo” and “halogen” as used herein refer to an atom selectedfrom fluorine (fluoro, —F), chlorine (chloro, —Cl), bromine (bromo,—Br), and iodine (iodo, —I).

The term “aliphatic” or “aliphatic group”, as used herein, denotes ahydrocarbon moiety that may be straight-chain (i.e., unbranched),branched, or cyclic (including fused, bridging, and spiro-fusedpolycyclic) and may be completely saturated or may contain one or moreunits of unsaturation, but which is not aromatic. Unless otherwisespecified, aliphatic groups contain 1-30 carbon atoms. In someembodiments, aliphatic groups contain 1-12 carbon atoms. In someembodiments, aliphatic groups contain 1-8 carbon atoms. In someembodiments, aliphatic groups contain 1-6 carbon atoms. In someembodiments, aliphatic groups contain 1-5 carbon atoms, in someembodiments, aliphatic groups contain 1-4 carbon atoms, in yet otherembodiments aliphatic groups contain 1-3 carbon atoms, and in yet otherembodiments, aliphatic groups contain 1-2 carbon atoms. Suitablealiphatic groups include, but are not limited to, linear or branched,alkyl, alkenyl, and alkynyl groups, and hybrids thereof such as(cycloalkyl)alkyl, (cycloalkenyl)alkyl or (cycloalkyl)alkenyl.

The term “heteroaliphatic,” as used herein, refers to aliphatic groupswherein one or more carbon atoms are independently replaced by one ormore atoms selected from the group consisting of oxygen, sulfur,nitrogen, phosphorus, or boron. In some embodiments, one or two carbonatoms are independently replaced by one or more of oxygen, sulfur,nitrogen, or phosphorus. Heteroaliphatic groups may be substituted orunsubstituted, branched or unbranched, cyclic or acyclic, and include“heterocycle,” “heterocyclyl,” “heterocycloaliphatic,” or “heterocyclic”groups.

The term “acrylate” or “acrylates” as used herein refer to any acylgroup having a vinyl group adjacent to the acyl carbonyl. The termsencompass mono-, di- and tri-substituted vinyl groups. Examples ofacrylates include, but are not limited to: acrylate, methacrylate,ethacrylate, cinnamate (3-phenylacrylate), crotonate, tiglate, andsenecioate.

The term “polymer”, as used herein, refers to a molecule of highrelative molecular mass, the structure of which comprises the multiplerepetitions of units derived, actually or conceptually, from moleculesof low relative molecular mass. In some embodiments, a polymer iscomprised of only one monomer species (e.g., polyethylene oxide). Insome embodiments, a polymer is a copolymer, terpolymer, heteropolymer,block copolymer, or tapered heteropolymer of one or more epoxides.

The term “unsaturated”, as used herein, means that a moiety has one ormore double or triple bonds.

The terms “cycloaliphatic”, “carbocycle”, or “carbocyclic”, used aloneor as part of a larger moiety, refer to a saturated or partiallyunsaturated cyclic aliphatic monocyclic, bicyclic, or polycyclic ringsystems, as described herein, having from 3 to 12 members, wherein thealiphatic ring system is optionally substituted as defined above anddescribed herein. Cycloaliphatic groups include, without limitation,cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl,cyclohexenyl, cycloheptyl, cycloheptenyl, cyclooctyl, cyclooctenyl, andcyclooctadienyl. In some embodiments, the cycloalkyl has 3-6 carbons.The terms “cycloaliphatic”, “carbocycle” or “carbocyclic” also includealiphatic rings that are fused to one or more aromatic or nonaromaticrings, such as decahydronaphthyl or tetrahydronaphthyl, where theradical or point of attachment is on the aliphatic ring. In someembodiments, a carbocyclic group is bicyclic. In some embodiments, acarbocyclic group is tricyclic. In some embodiments, a carbocyclic groupis polycyclic.

The term “alkyl,” as used herein, refers to saturated, straight- orbranched-chain hydrocarbon radicals derived from an aliphatic moietycontaining between one and six carbon atoms by removal of a singlehydrogen atom. Unless otherwise specified, alkyl groups contain 1-12carbon atoms. In some embodiments, alkyl groups contain 1-8 carbonatoms. In some embodiments, alkyl groups contain 1-6 carbon atoms. Insome embodiments, alkyl groups contain 1-5 carbon atoms, in someembodiments, alkyl groups contain 1-4 carbon atoms, in yet otherembodiments, alkyl groups contain 1-3 carbon atoms, and in yet otherembodiments alkyl groups contain 1-2 carbon atoms. Examples of alkylradicals include, but are not limited to, methyl, ethyl, n-propyl,isopropyl, n-butyl, iso-butyl, sec-butyl, sec-pentyl, iso-pentyl,tert-butyl, n-pentyl, neopentyl, n-hexyl, sec-hexyl, n-heptyl, n-octyl,n-decyl, n-undecyl, dodecyl, and the like.

The term “alkenyl,” as used herein, denotes a monovalent group derivedfrom a straight- or branched-chain aliphatic moiety having at least onecarbon-carbon double bond by the removal of a single hydrogen atom.Unless otherwise specified, alkenyl groups contain 2-12 carbon atoms. Insome embodiments, alkenyl groups contain 2-8 carbon atoms. In someembodiments, alkenyl groups contain 2-6 carbon atoms. In someembodiments, alkenyl groups contain 2-5 carbon atoms, in someembodiments, alkenyl groups contain 2-4 carbon atoms, in yet otherembodiments, alkenyl groups contain 2-3 carbon atoms, and in yet otherembodiments alkenyl groups contain 2 carbon atoms. Alkenyl groupsinclude, for example, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl,and the like.

The term “alkynyl,” as used herein, refers to a monovalent group derivedfrom a straight- or branched-chain aliphatic moiety having at least onecarbon-carbon triple bond by the removal of a single hydrogen atom.Unless otherwise specified, alkynyl groups contain 2-12 carbon atoms. Insome embodiments, alkynyl groups contain 2-8 carbon atoms. In someembodiments, alkynyl groups contain 2-6 carbon atoms. In someembodiments, alkynyl groups contain 2-5 carbon atoms, in someembodiments, alkynyl groups contain 2-4 carbon atoms, in yet otherembodiments alkynyl groups contain 2-3 carbon atoms, and in yet otherembodiments alkynyl groups contain 2 carbon atoms. Representativealkynyl groups include, but are not limited to, ethynyl, 2-propynyl(propargyl), 1-propynyl, and the like.

The term “carbocycle” and “carbocyclic ring” as used herein, refers tomonocyclic and polycyclic moieties wherein the rings contain only carbonatoms. Unless otherwise specified, carbocycles may be saturated,partially unsaturated or aromatic, and contain 3 to 20 carbon atoms.Representative carbocyles include cyclopropane, cyclobutane,cyclopentane, cyclohexane, bicyclo[2,2,1]heptane, norbornene, phenyl,cyclohexene, naphthalene, and spiro[4.5]decane.

The term “aryl” used alone or as part of a larger moiety as in“aralkyl”, “aralkoxy”, or “aryloxyalkyl”, refers to monocyclic andpolycyclic ring systems having a total of five to 20 ring members,wherein at least one ring in the system is aromatic and wherein eachring in the system contains three to twelve ring members. The term“aryl” may be used interchangeably with the term “aryl ring”. In someembodiments, “aryl” refers to an aromatic ring system which includes,but is not limited to, phenyl, naphthyl, anthracyl and the like, whichmay bear one or more substituents. Also included within the scope of theterm “aryl”, as it is used herein, is a group in which an aromatic ringis fused to one or more additional rings, such as benzofuranyl, indanyl,phthalimidyl, naphthimidyl, phenanthridinyl, or tetrahydronaphthyl, andthe like.

The terms “heteroaryl” and “heteroar-”, used alone or as part of alarger moiety, e.g., “heteroaralkyl”, or “heteroaralkoxy”, refer togroups having 5 to 14 ring atoms, preferably 5, 6, 9 or 10 ring atoms;having 6, 10, or 14 □ electrons shared in a cyclic array; and having, inaddition to carbon atoms, from one to five heteroatoms. The term“heteroatom” refers to nitrogen, oxygen, or sulfur, and includes anyoxidized form of nitrogen or sulfur, and any quaternized form of a basicnitrogen. Heteroaryl groups include, without limitation, thienyl,furanyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl,oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl,thiadiazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, indolizinyl,purinyl, naphthyridinyl, benzofuranyl and pteridinyl. The terms“heteroaryl” and “heteroar-”, as used herein, also include groups inwhich a heteroaromatic ring is fused to one or more aryl,cycloaliphatic, or heterocyclyl rings, where the radical or point ofattachment is on the heteroaromatic ring. Non-limiting examples includeindolyl, isoindolyl, benzothienyl, benzofuranyl, dibenzofuranyl,indazolyl, benzimidazolyl, benzthiazolyl, quinolyl, isoquinolyl,cinnolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, 4H-quinolizinyl,carbazolyl, acridinyl, phenazinyl, phenothiazinyl, phenoxazinyl,tetrahydroquinolinyl, tetrahydroisoquinolinyl, andpyrido[2,3-b]-1,4-oxazin-3(4H)-one. A heteroaryl group may be monocyclicor bicyclic. The term “heteroaryl” may be used interchangeably with theterms “heteroaryl ring”, “heteroaryl group”, or “heteroaromatic”, any ofwhich terms include rings that are optionally substituted. The term“heteroaralkyl” refers to an alkyl group substituted by a heteroaryl,wherein the alkyl and heteroaryl portions independently are optionallysubstituted.

As used herein, the terms “heterocycle”, “heterocyclyl”, “heterocyclicradical”, and “heterocyclic ring” are used interchangeably and refer toa stable 5- to 7-membered monocyclic or 7- to 14-membered bicyclicheterocyclic moiety that is either saturated or partially unsaturated,and having, in addition to carbon atoms, one or more, preferably one tofour, heteroatoms, as defined above. When used in reference to a ringatom of a heterocycle, the term “nitrogen” includes a substitutednitrogen. As an example, in a saturated or partially unsaturated ringhaving 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, thenitrogen may be N (as in 3,4-dihydro-2H-pyrrolyl), NH (as inpyrrolidinyl), or ⁺NR (as in N-substituted pyrrolidinyl).

A heterocyclic ring can be attached to its pendant group at anyheteroatom or carbon atom that results in a stable structure and any ofthe ring atoms can be optionally substituted. Examples of such saturatedor partially unsaturated heterocyclic radicals include, withoutlimitation, tetrahydrofuranyl, tetrahydrothienyl, pyrrolidinyl,pyrrolidonyl, piperidinyl, pyrrolinyl, tetrahydroquinolinyl,tetrahydroisoquinolinyl, decahydroquinolinyl, oxazolidinyl, piperazinyl,dioxanyl, dioxolanyl, diazepinyl, oxazepinyl, thiazepinyl, morpholinyl,and quinuclidinyl. The terms “heterocycle”, “heterocyclyl”,“heterocyclyl ring”, “heterocyclic group”, “heterocyclic moiety”, and“heterocyclic radical”, are used interchangeably herein, and alsoinclude groups in which a heterocyclyl ring is fused to one or morearyl, heteroaryl, or cycloaliphatic rings, such as indolinyl,3H-indolyl, chromanyl, phenanthridinyl, or tetrahydroquinolinyl, wherethe radical or point of attachment is on the heterocyclyl ring. Aheterocyclyl group may be mono- or bicyclic. The term“heterocyclylalkyl” refers to an alkyl group substituted by aheterocyclyl, wherein the alkyl and heterocyclyl portions independentlyare optionally substituted.

As used herein, the term “partially unsaturated” refers to a ring moietythat includes at least one double or triple bond. The term “partiallyunsaturated” is intended to encompass rings having multiple sites ofunsaturation, but is not intended to include aryl or heteroarylmoieties, as herein defined.

As described herein, compounds may contain “optionally substituted”moieties. In general, the term “substituted”, whether preceded by theterm “optionally” or not, means that one or more hydrogens of thedesignated moiety are replaced with a suitable substituent. Unlessotherwise indicated, an “optionally substituted” group may have asuitable substituent at each substitutable position of the group, andwhen more than one position in any given structure may be substitutedwith more than one substituent selected from a specified group, thesubstituent may be either the same or different at every position.Combinations of substituents envisioned may include those that result inthe formation of stable or chemically feasible compounds. The term“stable”, as used herein, refers to compounds that are not substantiallyaltered when subjected to conditions to allow for their production,detection, and, in some embodiments, their recovery, purification, anduse for one or more of the purposes disclosed herein.

In some chemical structures herein, substituents are shown attached to abond which crosses a bond in a ring of the depicted molecule. This meansthat one or more of the substituents may be attached to the ring at anyavailable position (usually in place of a hydrogen atom of the parentstructure). In cases where an atom of a ring so substituted has twosubstitutable positions, two groups may be present on the same ringatom. When more than one substituent is present, each is definedindependently of the others, and each may have a different structure. Incases where the substituent shown crossing a bond of the ring is —R,this has the same meaning as if the ring were said to be “optionallysubstituted” as described in the preceding paragraph.

Suitable monovalent substituents on a substitutable carbon atom of an“optionally substituted” group are independently halogen;—(CH₂)₀₋₄R^(∘); —(CH₂)₀₋₄OR^(∘); —O—(CH₂)₀₋₄C(O)OR^(∘);—(CH₂)₀₋₄CH(OR^(∘))₂; —(CH₂)₀₋₄SR^(∘); —(CH₂)₀₋₄Ph, which may besubstituted with R^(∘); —(CH₂)₀₋₄O(CH₂)₀₋₁Ph which may be substitutedwith R^(∘); —CH═CHPh, which may be substituted with R^(∘); —NO₂; —CN;—N₃; —(CH₂)₀₋₄N(R^(∘))₂; —(CH₂)₀₋₄N(R^(∘))C(O)R^(∘); —N(R^(∘))C(S)R^(∘);—(CH₂)₀₋₄N(R^(∘))C(O)NR^(∘) ₂; —N(R^(∘))C(S)NR^(∘) ₂;—(CH₂)₀₋₄N(R^(∘))C(O)OR^(∘); —N(R^(∘))N(R^(∘))C(O)R^(∘);—N(R^(∘))N(R^(∘))C(O)NR^(∘) ₂; —N(R^(∘))N(R^(∘))C(O)OR^(∘);—(CH₂)₀₋₄C(O)R^(∘); —C(S)R^(∘); —(CH₂)₀₋₄(O)OR^(∘);—(CH₂)₀₋₄C(O)N(R^(∘))₂; (—CH₂)₀₋₄C(O)SR^(∘); —(CH₂)₀₋₄(O)OSiR^(∘) ₃;—(CH₂)₀₋₄OC(O)R^(∘); —OC(O)(CH₂)₀₋₄SR^(∘), —SC(S)SR^(∘);—(CH₂)₀₋₄SC(O)R^(∘); —(CH₂)₀₋₄C(O)NR^(∘) ₂; —C(S)NR^(∘) ₂; —C(S)SR^(∘);—SC(S)SR^(∘), —(CH₂)₀₋₄OC(O)NR^(∘) ₂; —C(O)N(OR^(∘))R^(∘);—C(O)C(O)R^(∘); —C(O)CH₂C(O)R^(∘); —C(NOR^(∘))R^(∘); —(CH₂)₀₋₄SSR^(∘);—(CH₂)₀₋₄S(O)₂R^(∘); —(CH₂)₀₋₄S(O)₂OR^(∘); —(CH₂)₀₋₄OS(O)₂R^(∘);—S(O)₂NR^(∘) ₂; —(CH₂)₀₋₄S(O)R^(∘); —N(R^(∘))S(O)₂NR^(∘) ₂;—N(R^(∘))S(O)²R^(∘); —N(OR^(∘))R^(∘); —C(NH)NR^(∘) ₂; —P(O)₂R^(∘);—P(O)R^(∘) ₂; —OP(O)R^(∘) ₂; —OP(O)(OR^(∘))₂; SiR^(∘) ₃; —(C₁₋₄ straightor branched)alkylene)O—N(R^(∘))₂; or —(C₁₋₄ straight orbranched)alkylene)C(O)O—N(R^(◯))₂, wherein each R^(∘) may be substitutedas defined below and is independently hydrogen, C₁₋₈ aliphatic, —CH₂Ph,—O(CH₂)₀₋₁Ph, or a 5-6-membered saturated, partially unsaturated, oraryl ring having 0-4 heteroatoms independently selected from nitrogen,oxygen, and sulfur, or, notwithstanding the definition above, twoindependent occurrences of R^(∘), taken together with their interveningatom(s), form a 3-12-membered saturated, partially unsaturated, or arylmono- or polycyclic ring having 0-4 heteroatoms independently selectedfrom nitrogen, oxygen, and sulfur, which may be substituted as definedbelow.

Suitable monovalent substituents on R^(∘) (or the ring formed by takingtwo independent occurrences of R^(∘) together with their interveningatoms), are independently halogen, —(CH₂)₀₋₂R^(●), -(haloR^(●)),—(CH₂)₀₋₂OH, —(CH₂)₀₋₂OR^(●), —(CH₂)₀₋₂CH(OR^(●))₂; —O(haloR^(●)), —CN,—N₃, —(CH₂)₀₋₂C(O)R^(●), —(CH₂)₀₋₂C(O)OH, —(CH₂)₀₋₂C(O)OR^(●),—(CH₂)₀₋₄(O)N(R^(●) ₂; —(CH₂)₀₋₂SR^(●), —(CH₂)₀₋₂SH, —(CH₂)₀₋₂NH₂,—(CH₂)₀₋₂NHR^(●), —(CH₂)₀₋₂NR^(●) ₂, —NO₂, —SiR^(●) ₃, —OSiR^(●) ₃,—C(O)SR^(●), —(C₁₋₄ straight or branched alkylene)C(O)OR^(●), or—SSR^(●) wherein each R^(●) is unsubstituted or where preceded by “halo”is substituted only with one or more halogens, and is independentlyselected from C₁₋₄ aliphatic, —CH₂Ph, —O(CH₂)₀₋₁Ph, or a 5-6-memberedsaturated, partially unsaturated, or aryl ring having 0-4 heteroatomsindependently selected from nitrogen, oxygen, and sulfur. Suitabledivalent substituents on a saturated carbon atom of R^(∘) include ═O and═S.

Suitable divalent substituents on a saturated carbon atom of an“optionally substituted” group include the following: ═O, ═S, ═NNR*₂,═NNHC(O)R*, ═NNHC(O)OR*, ═NNHS(O)₂R*, ═NR*, ═NOR*, —O(C(R*₂))₂₋₃O—, or—S(C(R*₂))₂₋₃S—, wherein each independent occurrence of R* is selectedfrom hydrogen, C₁₋₆ aliphatic which may be substituted as defined below,or an unsubstituted 5-6-membered saturated, partially unsaturated, oraryl ring having 0-4 heteroatoms independently selected from nitrogen,oxygen, and sulfur. Suitable divalent substituents that are bound tovicinal substitutable carbons of an “optionally substituted” groupinclude: —O(CR*₂)₂₋₃O—, wherein each independent occurrence of R* isselected from hydrogen, C₁₋₆ aliphatic which may be substituted asdefined below, or an unsubstituted 5-6-membered saturated, partiallyunsaturated, or aryl ring having 0-4 heteroatoms independently selectedfrom nitrogen, oxygen, and sulfur.

Suitable substituents on the aliphatic group of R* include halogen,—R^(●), -(haloR^(●)), —OH, —OR^(●), —O(haloR^(●)), —CN, —C(O)OH,—C(O)OR^(●), —NH₂, —NHR^(●), —NR^(●) ₂, or —NO₂, wherein each R^(●) isunsubstituted or where preceded by “halo” is substituted only with oneor more halogens, and is independently C₁₋₄ aliphatic, —CH₂Ph,—O(CH₂)₀₋₁Ph, or a 5-6-membered saturated, partially unsaturated, oraryl ring having 0-4 heteroatoms independently selected from nitrogen,oxygen, and sulfur.

Suitable substituents on a substitutable nitrogen of an “optionallysubstituted” group include —R^(†), —NR^(†) ₂, —C(O)R^(†), —C(O)OR^(†),—C(O)C(O)R^(†), —C(O)CH₂C(O)R^(†), —S(O)₂R^(†), —S(O)₂NR^(†) ₂,—C(S)NR^(†) ₂, —C(NH)NR^(†) ₂, or —N(R^(†))S(O)₂R^(†); wherein eachR^(†) is independently hydrogen, C₁₋₆ aliphatic which may be substitutedas defined below, unsubstituted —OPh, or an unsubstituted 5-6-memberedsaturated, partially unsaturated, or aryl ring having 0-4 heteroatomsindependently selected from nitrogen, oxygen, and sulfur, or,notwithstanding the definition above, two independent occurrences ofR^(†), taken together with their intervening atom(s) form anunsubstituted 3-12-membered saturated, partially unsaturated, or arylmono- or bicyclic ring having 0-4 heteroatoms independently selectedfrom nitrogen, oxygen, and sulfur.

Suitable substituents on the aliphatic group of R^(†) are independentlyhalogen, —R^(†), -(haloR^(†)), —OH, —OR^(†), —O(haloR^(†)), —CN,—C(O)OH, —C(O)OR^(†), —NH₂, —NHR^(†), —NR^(†) ₂, or —NO₂, wherein eachR^(†) is unsubstituted or where preceded by “halo” is substituted onlywith one or more halogens, and is independently C₁₋₄ aliphatic, —CH₂Ph,—O(CH₂)₀₋₁Ph, or a 5-6-membered saturated, partially unsaturated, oraryl ring having 0-4 heteroatoms independently selected from nitrogen,oxygen, and sulfur.

As used herein, the term “catalyst” refers to a substance the presenceof which increases the rate of a chemical reaction, while not beingconsumed or undergoing a permanent chemical change itself.

As used herein, the term “about” preceding one or more numerical valuesmeans the numerical value ±5%. It should be understood that reference to“about” a value or parameter herein includes (and describes) embodimentsthat are directed to that value or parameter per se. For example,description referring to “about x” includes description of “x” per se.

Further, it should be understood that reference to “between” two valuesor parameters herein includes (and describes) embodiments that includethose two values or parameters per se. For example, descriptionreferring to “between x and y” includes description of “x” and “y” perse.

The mass fractions disclosed herein can be converted to wt % bymultiplying by 100.

Glacial Acrylic Acid Production System/Production Process

Glacial acrylic acid can be produced from ethylene oxide and carbonmonoxide according to the following general reaction scheme:

Ethylene oxide (“EO”) may undergo a carbonylation reaction, e.g., withcarbon monoxide (“CO”), in the present of a carbonylation catalyst toproduce β-propiolactone (“bPL”). The β-propiolactone may undergopolymerization in the presence of a polymerization catalyst to producepolypropiolactone (“PPL”). The polypropiolactone may undergo thermolysisto produce glacial acrylic acid (“GAA”).

PPL may undergo thermolysis by one of two primary reaction mechanisms asdisclosed by (Iwabuchi, S., Jaacks, V., Galil, F. and Kern, W. (1973),The thermal degradation of poly(oxycarbonylethylene)(poly-β-propiolactone). Makromol. Chem., 165: 59-72). The desiredmechanism is referred to as unzipping and it converts a PPL polymer witha chain length of “n” into one molecule of acrylic acid and reduces thePPL polymer chain length to n−1. The other method is referred to aschain scission; chain scission converts a PPL polymer of chain length ninto a PPL polymer of chain length of less than n−2 and a PPL polymer ofchain length of at least 2.

Product acrylic acid is susceptible to auto-polymerization via twomechanisms, either Michael addition or radical polymerization. Michaeladdition forms a product of two molecules of acrylic acid which is adi-acrylic acid ester and identical to a PPL of chain length 2. There isno known inhibitor of Michael addition of acrylic acid, but underthermolysis conditions this reaction is reversible and can decomposeback into two molecules of acrylic acid. The product of Radicalpolymerization of acrylic acid produces polyacrylic acid, and will notnormally convert back into acrylic acid under thermolysis conditions.There are many known inhibitors for radical polymerization of acrylicacid, including but not limited to phenothiazine (PTZ) and4-methoxyphenol (MEHQ). Under many circumstances, a stream of radicalpolymerization inhibitor (either neat or in appropriate solvent) isadded in batch or continuous mode to the primary thermolysis reactor ormixed with PPL stream before introduction to reactor to combat losses ofacrylic acid to polyacrylic acid in thermolysis reactor.

Thermolysis of PPL may be catalyzed by the presence of adepolymerization catalyst. Depolymerization catalyst (either neat or inappropriate solvent) may be added in batch or continuous mode to theprimary thermolysis reactor or mixed with PPL stream before introductionto reactor to reduce severity of thermolysis reaction conditions (whichreduces conversion of acrylic acid to polyacrylic acid). Optimally, thecatalyst employed for bPL polymerization can be used as adepolymerization catalyst as well. The thermolysis reactor can bedesigned (see below) such that the concentrations of the polymerizationcatalyst species in the PPL inlet stream and in the thermolysis reactor,which along with the difference in reactor conditions and streamcompositions accounts for the seemingly divergent functions.

Provided herein are systems and methods for the production of glacialacrylic acid from ethylene oxide and carbon monoxide on an industrialscale. For example, in some aspects, the systems and methods describedherein are suitable for the production of glacial acrylic acid on ascale of 25 kilo tons per annum (“KTA”). In some variations, the systemsprovided herein are configured to produce glacial acrylic acid in acontinuous process, and further feedback loops to continually produceacrylic acid.

Further, in some variations, the systems provided herein further includevarious purification systems to produce glacial acrylic acid of highpurity. For example, the systems provided herein may be configured toremove residual carbonylation catalyst, carbonylation solvent, andby-products (e.g., acetaldehyde, succinic anhydride, and acrylic aciddimer) to achieve glacial acrylic acid with a purity of at least 99.5%,at least 99.6%, at least 99.7%, at least 99.8%, or at least 99.9%.

In other variations, the systems provided herein are also configured torecycle various starting materials and glacial acrylic acid precursors,such as poly-propiolactone. For example, the systems may include one ormore recycle systems to isolate unreacted ethylene oxide, unreactedcarbon monoxide, carbonylation solvent, and catalyst.

In yet other variations, the systems provided herein are also configuredto manage and integrate heat produced. The carbonylation reaction toproduce β-propiolactone and the polymerization reaction to producepolypropiolactone are exothermic. Thus, the heat generated from theexothermic unit operations, such as the carbonylation reactor andpolymerization reactor can be captured and used for cooling inendothermic unit operations, such as the distillation apparatus andthermolysis reactor. For example, in some variations of the systems andmethods provided herein, steam may be generated in heat transferequipment (e.g., shell and tube heat exchanger and reactor coolingjacket) via a temperature gradient between process fluid andwater/steam. This steam can be used for heat integration betweenexothermic and endothermic unit operations. In other variations of thesystems and methods provided herein, other suitable heat transfer fluidsmay be used.

In other variations, heat integration may be achieved by combiningcertain unit operations. For example, heat integration may be achievedby combining polymerization of β-propiolactone and vaporization of thesolvent (e.g., THF) from the distillation column within a single unitoperation. In such a configuration, the heat liberated from theβ-propiolactone polymerization reaction is used directly to vaporize thesolvent in the distillation apparatus, and the output of the unitproduces polypropiolactone. In other variations, the heat liberated fromthe polymerization reaction can be exported to other systems at the sameproduction site.

With reference to FIG. 1, an exemplary system to produce acrylic acidfrom carbon monoxide and ethylene oxide is depicted. Carbon monoxide(CO), a carbonylation catalyst, ethylene oxide (EO) and carbonylationsolvent are fed into a β-propiolactone production system/productionprocess, depicted as a continuous stirred tank reactor (CSTR) in FIG. 1.Such β-propiolactone production system/production process is typicallyconfigured to produce a liquid product stream of β-propiolactone. Thisβ-propiolactone product stream is fed to an EO/CO separator, depicted asthe flash tank in FIG. 1, where unreacted ethylene oxide and unreactedcarbon monoxide may be separated and recycled for use in the CSTR. Theβ-propiolactone product stream is then fed from the EO/CO separator to acarbonylation catalyst recycle system, depicted as a nanofilter inFIG. 1. The carbonylation catalyst recycle system is configured toseparate residual carbonylation catalyst present in the β-propiolactoneproduct stream, and such separated carbonylation catalyst may berecycled for use in the CSTR. The nanofilter depicted in FIG. 1 may beany suitable membrane, such as a polymeric membrane or a ceramicmembrane, and produces a retentate stream typically made up ofβ-propiolactone, carbonylation solvent, residual carbonylation catalyst,small amounts of ethylene oxide, carbon monoxide, and by-products (suchas acetaldehyde and succinic anhydride), and a permeate stream typicallymade up of β-propiolactone, carbonylation solvent, small amounts ofethylene oxide, carbon monoxide, by-products (such as acetaldehyde andsuccinic anhydride) and trace amounts of carbonylation catalyst. In someembodiments, trace amount is less than 1% by wt, less than 0.5% by wt,less than 0.01% by wt, less than 0.005% by wt, less than 0.001% by wt,or less than 0.0001% by wt. In certain embodiments, trace amount isbelow the detection threshold of the measurement method being used.

The permeate is fed into a β-propiolactone purification system, depictedas a distillation column in FIG. 1, which is configured to separateethylene oxide, carbon monoxide, and by-products from the solventrecycle stream, which is depicted as a tetrahydrofuran (THF) recyclestream. The system in FIG. 1 depicts the use of THF as the carbonylationsolvent, but it should be understood that in other variations, othersuitable solvents may be used. The purified β-propiolactone stream fromthe β-propiolactone purification system and polymerization catalyst arefed into a polypropiolactone production system/production process,depicted as a plug flow reactor in FIG. 1. The polypropiolactoneproduction system/production process is configured to produce apolypropiolactone product stream, which can be fed into a thermolysisreactor to produce glacial acrylic acid.

FIG. 1 depicts an exemplary glacial acrylic acid productionsystem/production process, variations of this productions system areenvisioned. For example, while a CSTR is depicted as the reactor in theβ-propiolactone production system/production process, other reactors andreactor configurations may be employed. In another example, while adistillation column and a plug flow reactor are depicted in FIG. 1 inthe β-propiolactone purification system and polypropiolactoneproductions system, respectively, other separation apparatuses and otherreactors and reactor configurations may be employed.

Additionally, in other exemplary embodiments of the systems describedherein, various unit operations depicted in FIG. 1 may be combined oromitted. In some variations, the β-propiolactone productionsystem/production process and membrane unit operations may be combined(e.g. membrane reactor) or polymerization and depolymerization may becombined (e.g. catalytic or reactive distillation) may be combined, orthe EO/CO separator may be omitted.

Further, it should be understood that in other exemplary embodiments ofsystems described herein, additional unit operations may be employed.For example, in some embodiments it may be possible to incorporate oneor more ion exchange resins into the systems to remove various cationicand anionic catalyst species that may result from the use of thecarbonylation catalyst. In other embodiments, one or more heatexchangers may be incorporated into the systems to manage and integrateheat produced in the system.

In yet other embodiments the process and/or system by which it ispracticed may employ a variety of sensors and control equipment toautomate control of the process and any related system. For example, thevarious reactors, in particular a β-propiolactone reactor, used in theprocess and any related system may employ a sensor to detect amounts ofwater and oxygen in the reactor or that enters the reactor. Such sensormay be connected to a control that can adjust parameters to maintainwater and oxygen content under a predefined amount. Such sensor maymonitor the carbonylation catalyst to detect amounts of water and oxygenin the reactor and may be connected to a control that can control theamount of carbonylation catalyst from the carbonylation catalyst source.In addition, or alternatively the carbon monoxide source may comprise asensor configured to detect amounts of water and oxygen in the reactorand such sensor may be connected to a control that can control theamount of carbon monoxide from the carbon monoxide source. In addition,or alternatively the ethylene oxide source may comprises a sensorconfigured to detect amounts of water and oxygen in the reactor and suchsensor may be connected to a control that can control the amount ofethylene oxide from the ethylene oxide source.

Provided herein are various systems configured for the commercialproduction of polypropiolactone (PPL) and glacial acrylic acid (GAA). Insome configurations, PPL and GAA are produced at the same geographicallocation. In other configurations, PPL is produced in one location andshipped to a second location where GAA is produced.

In other variations of such configurations, the residual carbonylationcatalyst (which may include cationic and anionic species) may be removedat various points in the production system/production process. Forexample, in certain configurations, the residual carbonylation catalystmay be removed from the PPL product stream prior to thermolysis toproduce GAA. In other configurations, the residual carbonylationcatalyst may be removed, if desired to do so, after thermolysis bydistillation or other separation means.

In yet other variations, β-propiolactone (bPL) may be polymerized toproduce PPL by way of complete conversion of bPL. In such a variation,there may not be a need for additional apparatus in the system toisolate and recycle bPL to the polymerization reactor. In othervariations, the conversion of bPL is not complete. Unreacted bPL may beseparated from the PPL product stream and the recovered bPL may berecycled back to the polymerization reactor.

These variations in the configurations of the systems are described infurther detail with respect to FIGS. 6-13. FIG. 6 depicts an exemplarysystem wherein the PPL product stream and the GAA product stream areproduced at the same location, at least a portion of the carbonylationcatalyst or components thereof are removed from the PPL product streamprior to entering the thermolysis reactor, and the polypropiolactoneproduction system/production process is configured to achieve completeconversion of bPL to PPL.

Carbonylation catalyst components may include, for example, compoundsproduced by degradation of the catalyst, compounds used to produce thecatalyst, metals or metal ions which were part of the catalyst, anyorganic compounds which were part of the catalyst, metal carbonyls ormetal complexes which were part of the catalyst. For example, in someembodiments, carbonylation catalyst components are carbonyl cobaltate,aluminum salen compounds, aluminum porphyrin compounds, aluminumsalophen compounds, cobalt or cobalt ions, or aluminum or aluminum ions,or any combinations thereof.

The BPL production system/production process (labeled ‘Carbonylation’ inFIG. 6) typically includes a carbon monoxide (CO) source, an ethyleneoxide (EO) source, a carbonylation catalyst source, a solvent source,and a carbonylation reactor. In certain variations, the carbonylationreactor is configured to receive carbon monoxide (CO), ethylene oxide(EO), and solvent from a CO source, an EO source, and a solvent source(collectively labeled ‘Feed Stock Delivery’ in FIG. 6). Thecarbonylation reactor is further configured to receive a carbonylationcatalyst from a carbonylation catalyst source (labeled ‘CO CatalystDelivery’ in FIG. 6). The carbon monoxide, ethylene oxide, carbonylationsolvent, and carbonylation catalyst may be obtained by any commerciallyavailable sources, or any commercially available methods and techniquesknown in the art.

In some variations, the CO, EO, and solvent are essentially water andoxygen free. In one variation, the solvent from the solvent source, theEO from the EO source, and the CO from the CO source have aconcentration of water and oxygen less than about 500 ppm, less thanabout 250 ppm, less than about 100 ppm, less than about 50 ppm, lessthan about 10 ppm, less than about 2 ppm, or less than 1 ppm.

Any suitable carbonylation solvents may be used. In some embodiments,the carbonylation solvent comprises tetrahydrofuran, hexane, or acombination thereof. In other embodiments, the carbonylation solventcomprises an ether, a hydrocarbon, or a combination thereof. In yetother embodiments, the carbonylation solvent comprises tetrahydrofuran,tetrahydropyran, 2,5-dimethyl tetrahydrofuran, sulfolane, N-methylpyrrolidone, 1,3 dimethyl-2-imidazolidinone, diglyme, triglyme,tetraglyme, diethylene glycol dibutyl ether, isosorbide ethers, methyltertbutyl ether, diethylether, diphenyl ether, 1,4-dioxane, ethylenecarbonate, propylene carbonate, butylene carbonate, dibasic esters,diethyl ether, acetonitrile, ethyl acetate, propyl acetate, butylacetate, 2-butanone, cyclohexanone, toluene, difluorobenzene, dimethoxyethane, acetone, or methylethyl ketone, or any combination thereof. Inone variation, the carbonylation solvent comprises tetrahydrofuran.

The carbonylation catalyst used herein may be made on-site and/oroff-site. In some embodiments, the carbonylation catalyst is acobalt-aluminum catalyst. In certain embodiments, the carbonylationcatalyst comprises a carbonyl cobaltate in combination with an aluminumporphyrin compound, a carbonyl cobaltate in combination with an aluminumsalen compound, or a carbonyl cobaltate in combination with an aluminumsalophen compound. In one variation, the carbonylation catalyst is(Al(TPP)Co(CO)₄).

The carbonylation reactor may be a continuous reactor, such as acontinuous stirred tank reactor (CSTR). Other reactors described herein,such as batch reactors, plug flow reactors (PFR), and semi-batchreactors may also be employed.

With reference again to the exemplary system in FIG. 6, thecarbonylation reactor may be configured to receive EO from the EO sourceat any rate, temperature, or pressure described herein. For example, insome embodiments, the inlet to the carbonylation reactor receives EOfrom an EO source at about 1000 kg/hr to 25000 kg/hr. In someembodiments, the inlet to the carbonylation reactor receives EO from anEO source at about 30 kmol/hr to about 500 kmol/hr. In some embodiments,the inlet to the carbonylation reactor is configured to receive EO froman EO source at a temperature between about 10° C. to about 30° C. Insome embodiments, the inlet to the carbonylation reactor is configuredto receive EO from an EO source at a pressure between about 20 bar toabout 100 bar and in a more narrow range 50 bar to 70 bar.

With reference again to the exemplary system in FIG. 6, thecarbonylation reactor may be configured to receive CO from the CO sourceat any rate, temperature, or pressure described herein. For example, insome embodiments, the inlet to the carbonylation reactor is configuredto receive CO from a CO source at a temperature between about 10° C. toabout 170° C. and more narrowly between 10° C. to about 70° C. In someembodiments, the inlet to the carbonylation reactor is configured toreceive CO from a CO source at a pressure between about 20 bar to about100 bar and more narrowly 50 and 70 bar. In some embodiments, the COsource that supplies CO to the carbonylation reactor is a fresh carbonmonoxide source (i.e., main CO feed), or recycled carbon monoxide fromthe β-propiolactone production system/production process, or acombination thereof. In some embodiments, the fresh CO source isconfigured to provide between about 1000 kg/hr CO to about 16000 kg/hrCO. In some embodiments, the fresh CO source is configured to providebetween about 30 kmol/hr CO to about 600 kmol/hr CO. In someembodiments, the recycled CO from the β-propiolactone productionsystem/production process can provide between about 100 kg/hr CO toabout 3500 kg/hr CO. In some embodiments, the recycled CO source isconfigured to provide between about 3 kmol/hr CO to about 150 kmol/hrCO.

In FIG. 6, the carbonylation reactor may be configured to receivesolvent at any rate, temperature, or pressure described herein. Forexample, in some embodiments, the inlet to the carbonylation reactor isconfigured to receive solvent from a solvent feed at a rate of betweenabout 10000 kg/hr to about 130000 kg/hr. In some embodiments, the inletto the carbonylation reactor is configured to receive solvent from asolvent feed at rate of between about 150 kmol/hr to about 1900 kmol/hr.In some embodiments, the inlet to the carbonylation reactor isconfigured to receive solvent from a solvent feed at a temperaturebetween about 10° C. to about 160° C. and more narrowly 10° C. to about60° C. In some embodiments, the inlet to the carbonylation reactor isconfigured to receive solvent from a solvent feed at a pressure ofbetween about 20 bar to about 100 bar and more narrowly 50 bar to 65bar. In some embodiments, the solvent feed that supplies solvent to thecarbonylation reactor can include solvent from a fresh solvent source,recycled solvent from the BPL purification system (e.g., BPLdistillation system), and/or solvent in the recycled carbonylationcatalyst stream from the carbonylation catalyst recycle system.

In some embodiments, the pressure in the carbonylation reactor is about900 psig, and the temperature is about 70° C. In certain variations, thereactor is equipped with an external cooler (heat exchanger). In somevariations, the carbonylation reaction achieves a selectivity of bPLabove 99%.

With reference again to the exemplary system in FIG. 6, aβ-propiolactone product stream exits the outlet of the carbonylationreactor. The β-propiolactone product stream comprises bPL, solvent,unreacted EO and CO, carbonylation catalyst, and by-products, such asacetaldehyde by-product (ACH) and succinic anhydride (SAH). Theβ-propiolactone product stream may have any concentration of bPL,solvent, EO, CO carbonylation catalyst, ACH, and SAH described herein.For example, in some embodiments, the β-propiolactone product streamincludes between about 2000 kg/hr bPL to about 40000 kg/hr bPL. In someembodiments, the β-propiolactone product stream includes between about30 kmol/hr bPL to about 550 kmol/hr bPL. In some embodiments, the massfraction of bPL in the β-propiolactone product stream can be about 0.1to about 0.4. In some embodiments, the mole fraction of bPL in theβ-propiolactone product stream can be about 0.1 to about 0.6. and morenarrowly 0.1 to 0.4. The β-propiolactone product stream can also includeother components including unreacted ethylene oxide (in mass fraction ofabout 0.005 to 0.15, or at most about 0.1), unreacted carbon monoxide(in mass fraction of about 0.0005 to 0.04, or at most about 0.02),acetaldehyde (in mass fraction of about 0.0005 to 0.01, or at most about0.02), succinic anhydride (in mass fraction of about 0.0005 to 0.005, orat most about 0.01), carbonylation catalyst (in about 40 to 640 kg/hr,or at most about 600 kg/hr; or a mass fraction of about 0.001 to 0.005,or at most about 0.004), and the remainder solvent. In some embodiments,the β-propiolactone product stream comprises carbonylation catalystcomponents (in about 40 to 640 kg/hr, or at most about 600 kg/hr; or amass fraction of about 0.001 to 0.005, or at most about 0.004). In someembodiments, the β-propiolactone product stream from the β-propiolactoneproduction system/production process can have a temperature of about 40°C. or 50° C. to about 100° C., and a pressure of about 1 bar to about 15bar or more narrowly to 5 bar.

In FIG. 6, the β-propiolactone product stream is output from an outletof the carbonylation reactor and enters an inlet of the ethylene oxideand carbon monoxide separator (labeled ‘EO/CO’ in FIG. 6). In oneembodiment, the ethylene oxide and carbon monoxide separator is a flashtank. The majority of the ethylene oxide and carbon monoxide isrecovered from the carbonylation reaction stream and can be recycledback to the carbonylation reactor as a recycled ethylene oxide streamand a recycled carbon monoxide stream (labeled ‘Recycle’ in FIG. 6), orsent for disposal (labeled ‘Flare’ in FIG. 6). In some embodiments, atleast 10% of the ethylene oxide and 80% of the carbon monoxide in thecarbonylation reaction stream is recovered. The recycled carbon monoxidestream can also include unreacted ethylene oxide (in about at most 250kg/hr or a mass fraction of between about 0.05 to about 0.075),secondary reaction product acetaldehyde (in at most about 13 kg/hr or amass fraction of about 0.001 to about 0.009), bPL (in at most about 0.19kg/hr), and the remainder solvent (e.g., THF).

The exemplary system in FIG. 6, the β-propiolactone product stream ispumped into the carbonylation catalyst recycle system. In somevariations, the ethylene oxide and carbon monoxide are disposed of usinga method other than flare. For example, in one embodiment, the ethyleneoxide and carbon monoxide recovered from the β-propiolactone productstream are disposed of using incineration.

In FIG. 6, the β-propiolactone product stream enters an inlet of thecarbonylation catalyst recycling system. The carbonylation catalystrecycling system may be configured to isolate at least a portion of thecarbonylation catalyst from the β-propiolactone product stream using anyof the methods described herein, including, for example distillation,liquid-liquid extraction, ionic liquids, nanofiltration, ion exchange,or adsorption, or any combinations thereof. In some variations, thecarbonylation catalyst recycling system includes a membrane separator.In certain variations, the membrane separator comprises a polymericmembrane, while in other variations the membrane separator comprises aceramic membrane. In some variations, the membrane of the catalystrecycle system is configured to achieve between 90% and 100% rejectionof the catalyst, and have permeability greater than 1. In someembodiments the membrane is achieves greater than 90%, 92%, 95%, 98%, or99% rejection of the catalyst.

The carbonylation catalyst recycling system is configured to produce arecycled carbonylation catalyst stream (labeled ‘Retentate’ in FIG. 6)comprising bPL, solvent, ethylene oxide, carbon monoxide, by-products(such as acetaldehyde and carbonylation catalyst) and carbonylationcatalyst, and a post-isolation β-propiolactone product stream (labeled‘Permeate’ in FIG. 6) comprising bPL, solvent, ethylene oxide, carbonmonoxide, by-products (such as acetaldehyde and succinic anhydride) andtrace amounts of carbonylation catalyst. In some embodiments, thepost-isolation β-propiolactone product stream comprises trace amounts ofcarbonylation catalyst components. In some embodiments, trace amount isless than 1% by wt, less than 0.5% by wt, less than 0.01% by wt, lessthan 0.005% by wt, less than 0.001% by wt, or less than 0.0001% by wt.In certain embodiments, trace amount is below the detection threshold ofthe measurement method being used.

The recycled carbonylation catalyst stream may comprise anyconcentration of carbonylation catalyst, carbonylation catalystcomponents, and solvent disclosed herein. For example, in someembodiments, the mass fraction of carbonylation catalyst in the recycledcarbonylation catalyst stream is about 0.005 to about 0.05. In someembodiments, the mass fraction of carbonylation catalyst components inthe recycled carbonylation catalyst stream is about 0.0051 to about0.05. In some embodiments, the mole fraction of carbonylation catalystin the recycled carbonylation catalyst stream is about 0.0005 to about0.05. In some embodiments, the mole fraction of carbonylation catalystcomponents in the recycled carbonylation catalyst stream is about 0.0005to about 0.05. In some embodiments, the mass fraction of solvent in therecycled carbonylation catalyst stream is between 0.60 to about 0.99. Insome embodiments, the mole fraction of solvent in the recycledcarbonylation catalyst stream is between about 0.60 to about 0.99. Insome embodiments, the recycled carbonylation catalyst stream can alsoinclude unreacted carbon monoxide (in at most about 15 kg/hr or a massfraction of at most about 0.001), unreacted ethylene oxide (in at mostabout 330 kg/hr or a mass fraction of between 0.005 to 0.01), secondaryreaction product acetaldehyde (in at most about 33 kg/hr or a massfraction of at most about 0.001), secondary reaction product succinicanhydride (in at most about 30 kg/hr or a mass fraction of at most about0.001), bPL (in at most about 5450 kg/hr or a mass fraction of at mostabout 0.25). The recycled carbonylation catalyst stream is recycled backto the carbonylation reactor.

The post-isolation β-propiolactone product stream may have anyconcentration of bPL, solvent, ethylene oxide, carbon monoxide,by-products (such as acetaldehyde and succinic anhydride), carbonylationcatalyst, or carbonylation catalyst components described herein. Forexample, in some embodiments, the post-isolation β-propiolactone productstream includes about 2000 kg/hr bPL to about 35000 kg/hr bPL. In someembodiments, the post-isolation β-propiolactone product stream includesabout 30 kmol/hr bPL to about 450 kmol/hr bPL. In some embodiments, themass fraction of bPL in the post-isolation β-propiolactone productstream can be about 0.1 to 0.4, or the mole fraction of bPL in thepost-isolation β-propiolactone product stream can be about 0.1 to about0.4. The post-isolation β-propiolactone product stream can also includeother components including unreacted ethylene oxide (in mass fraction ofabout 0.005 to 0.1), unreacted carbon monoxide (in mass fraction ofabout 0.0005 to 0.001, or at most about 0.002), acetaldehyde (in massfraction of about 0.0005 to 0.001, or at most about 0.002), succinicanhydride (in mass fraction of about 0.0005 to 0.01, or at most about0.02), carbonylation catalyst (in about 0 to 50 kg/hr, or at most about20 kg/hr), carbonylation catalyst components (in about 0 to 50 kg/hr, orat most about 20 kg/hr) and the remainder solvent. In some embodiments,the post-isolation β-propiolactone product stream from the carbonylationcatalyst recycling system can have a temperature of about 20° C. toabout 60° C. In some embodiments, the post-isolation β-propiolactoneproduct stream can have a pressure of about 1 to about 5 bar.

The system in FIG. 6, the post-isolation β-propiolactone product streammay enter the inlet of the BPL purification system (labeled ‘BPLDistillation’ in FIG. 6). In one variation, the BPL purification systemcomprises one or more distillation columns operating at or belowatmospheric pressure configured to produce a recovered solvent stream,and a production stream comprising purified bPL and trace amounts ofcarbonylation catalyst (labeled ‘BPL/residual cat.’ in FIG. 6). Thepressure is selected in such a way to achieve the temperature thatreduces the decomposition of bPL. In some embodiments, the one or moredistillation columns are operated at a pressure of about 0.15 bara and atemperature between about 80° C. and about 120° C. In some embodiments,the distillation system is configured to produce a recycled solventstream essentially free of ethylene oxide, carbon monoxide,acetaldehyde, and succinic anhydride.

The exemplary system in FIG. 6, the recovered solvent stream exits anoutlet of the BPL purification system and may be fed back to thecarbonylation reactor. In some variations, the concentration of H₂O andO₂ is reduced in the recycled solvent stream prior to being fed to thecarbonylation reactor. The recovered solvent stream may have anyconcentration of H₂O and O₂ described herein when fed back to thecarbonylation reactor. For example, in some embodiments, theconcentration of H₂O and O₂ is less than about 500 ppm, less than about250 ppm, less than about 100 ppm, less than about 50 ppm, less thanabout 20 ppm, less than about 10 ppm, less than about 2 ppm, or lessthan about 1 ppm when fed back into the carbonylation reactor.

The system in FIG. 6, the production stream comprising purified bPLexits the outlet of the BPL purification system. The production streammay contain trace amounts of carbonylation catalyst, but is essentiallyfree of solvent, ethylene oxide, carbon monoxide, acetaldehyde, andsuccinic anhydride. In some embodiments, the production stream containsa mass fraction of bPL of about 0.90 to 1.0. In some embodiments, themole fraction of bPL in the production stream is about 0.90 to 1.0. Insome embodiments, the remainder of the production stream includessecondary reaction products such as succinic anhydride (in mole fractionof at most about 0.015, or from 0 to 0.0015), leftover solvent (e.g.,THF) and leftover carbonylation catalyst (in at most about 1000 ppm). Insome embodiments, the remainder of the production stream includescarbonylation catalyst components (in at most about 1000 ppm).

The production stream enters an inlet of the polypriolactone productionsystem/production process. The system depicted in FIG. 6, thepolypriolactone production system/production process comprises apolymerization reactor (labeled ‘Polymerization’ in FIG. 6). Thepolypriolactone production system/production process is configured toreceive and output streams at any rate, concentration, temperature, orpressure described herein. For example, in one embodiment, the inlet tothe polymerization process can include about 2000 kg/hr bPL to about35000 kg/hr bPL. In some embodiments, the inlet to the polymerizationprocess can include about 25 kmol/hr bPL to about 500 kmol/hr bPL. Insome embodiments, the mass fraction of bPL in the inlet to thepolymerization process can be about 0.90 to 1.0. In some embodiments,the mole fraction of bPL in the inlet to the polymerization process canbe from about 0.90 to 1.0. The remainder of the production streamentering the polymerization process can include secondary reactionproducts such as succinic anhydride (in mole fraction of at most about0.015, or from 0 to about 0.015), leftover solvent (e.g., THF) andleftover carbonylation catalyst (in at most about 1000 ppm). Theremainder of the production stream entering the polymerization processcan include carbonylation catalyst components (in at most about 1000ppm). In some embodiments, the inlet to the polymerization process canalso include a polymerization catalyst, for example, if thepolymerization reaction is a homogenous polymerization reaction. In someembodiments, the production stream entering the polymerization processcan have a temperature between about 80° C. to 120° C. In someembodiments, the production stream exiting the distillation process canbe at a pressure of about 0.05 bar to about 0.15 bar. In someembodiments, the production stream entering the polymerization processcan be at a pressure of at least about 0.05 bar, at least about 1 bar,or at least about 5 bar, or between about 0.05 bar and about 20 bar.

The system in FIG. 6, the polypropiolactone production system/productionprocess is configured to operate in a continuous mode and achievescomplete conversion of bPL in the production stream to PPL. A PPLproduct stream (labeled ‘PPL/residual cat.’ in FIG. 6) exits an outletof the polypropiolactone production system/production process, andcomprises PPL with trace amount of carbonylation catalyst. In someembodiments, the PPL product stream comprises trace amount ofcarbonylation catalyst components.

In some embodiments, the polymerization process is configured to produceabout 2000 kg/hr PPL to about 35000 kg/hr PPL. In some embodiments, thepolymerization process is configured to produce about 25 kmol/hr PPL toabout 500 kmol/hr PPL.

In some embodiments, the mass fraction of PPL in the PPL product streamcan be about 0.90 to 1.0. In some embodiments, the mole fraction of PPLin the PPL product stream can be about 0.90 to 1.0. The remainder of thePPL product stream can include unreacted bPL (in mole fraction of atmost about 0.02, or between 0 and 0.02), secondary reaction productssuch as succinic anhydride (in mole fraction of at most about 0.01, orbetween 0 and 0.01) and left over solvent (e.g., THF) and leftovercarbonylation catalyst (in at most about 1000 ppm). In some embodiments,the remainder of the PPL product stream can include carbonylationcatalyst components (in at most about 1000 ppm). In some embodiments,the PPL product stream can have a temperature between about 100° C. to140° C. In some embodiments, the PPL product stream can be at a pressureof at least about 0.001 bar.

The exemplary system in FIG. 6, the PPL product stream enters an inletof the PPL purification system (labeled ‘IER’ in FIG. 6). The PPLpurification system can comprises and ion exchange resin (IER)configured to reduce the concentration of carbonylation catalyst in thePPL product stream. The cationic and anionic carbonylation catalystspecies are recovered from the IER in the PPL purification system andcan be regenerated to obtain catalyst available for recycle to thecarbonylation reactor or be disposed of (labeled ‘Regenerate/Dispose’ inFIG. 6). A post-purification PPL product stream exits an outlet of thePPL purification system and enters an inlet of the thermolysis reactor.The post-purification PPL product stream may have any concentration ofcompounds, temperature, or pressure described herein. For example, insome embodiments, the mass fraction of PPL in the post-purification PPLproduct stream can be about 0.90 to 1.0. In some embodiments, the molefraction of PPL in the post-purification PPL product stream can be about0.90 to 1.0. In some embodiments, the post-purification PPL productstream can have a temperature between about 100° C. to 140° C. In someembodiments, the post-purification PPL product stream can be at apressure of at least about 0.001 bar.

The system in FIG. 6, a thermolysis reactor is configured to convert thepost-purification PPL stream to a GAA product stream. In someembodiments, the temperature of the thermolysis reactor is between 140°C. or 160° C. and 300° C. and the pressure is between 0.1 bara and 5bara.

Traces of high boiling organic impurities (labeled ‘Organic Heavies’ inFIG. 6) are separated from the GAA stream, exit an outlet of thethermolysis reactor, and sent to the incinerator for disposal (labeled‘Incinerator’ in FIG. 6).

A GAA product stream exits an outlet of the thermolysis reactor forstorage or further processing. The GAA product stream comprisesessentially pure GAA. The GAA product stream may exit an outlet of thethermolysis reactor at any rate, concentration, temperature, or pressuredescribed herein. The remainder of the GAA product stream can includesecondary reaction products such as succinic anhydride and left oversolvent such as THF. In some embodiments, the GAA product stream canhave a temperature between about 15° C. to about 50° C. In someembodiments, the GAA product stream can be at a pressure of about 0.5bar to about 1.5 bar.

The exemplary production system/production process depicted in FIG. 6may produce GAA at any rate described herein. For example, in someembodiments, the system produces at least about 25 kilo tons per annum(“KTA”) to about 250 KTA for annual production operation of about 8000hours. In some embodiments, the production system/production process canproduce at least about 2000 kg/hr GAA to about 35000 kg/hr GAA. In someembodiments, the production system/production process can produce about25 kmol/hr GAA to about 500 kmol/hr GAA.

FIG. 7 provides an exemplary production system/production process wherethe PPL product stream and the GAA product stream are produced at thesame location, at least a portion of the carbonylation catalyst orcomponents thereof are removed from the PPL product stream prior toentering the thermolysis reactor, and the conversion of bPL in theproduction stream to PPL in the polymerization reactor is incomplete,with recycling of bPL back to the polymerization reactor. The productionsystem/production process shown in FIG. 7 has the same configuration ofcarbonylation reactor, CO catalyst recycling, EO/CO recycling and BPLpurification system as shown in FIG. 6.

The exemplary system in FIG. 7, the production stream comprisingpurified bPL exits the outlet of the BPL purification system. Theproduction stream may contain trace amounts of carbonylation catalyst,but is essentially free of solvent, ethylene oxide, carbon monoxide,acetaldehyde, and succinic anhydride. In some embodiments, theproduction stream contains a mass fraction of bPL of about 0.90 to 1.0.In some embodiments, the mole fraction of bPL in the production streamis about 0.90 to 1.0. In some embodiments, the remainder of theproduction stream includes secondary reaction products such as succinicanhydride (in mole fraction of at most about 0.015) and left oversolvent (e.g., THF) and leftover carbonylation catalyst (in at mostabout 1000 ppm). In some embodiments, the remainder of the productionstream includes carbonylation catalyst components (in at most about 1000ppm).

The exemplary system in FIG. 7, the polypropiolactone productionsystem/production process comprises a polymerization reactor (labeled‘Polymerization’ in FIG. 7) and a BPL recycling system (labeledDistill/WFE′ in FIG. 7). The polypropiolactone productionsystem/production process may be configured to receive and outputstreams at any rate, concentration, temperature, or pressure ofproduction stream described herein. For example, in one embodiment, theinlet to the polymerization process can include about 2000 kg/hr bPL toabout 35000 kg/hr bPL. In some embodiments, the inlet to thepolymerization process can include about 25 kmol/hr bPL to about 500kmol/hr bPL. In some embodiments, the mass fraction of bPL in the inletto the polymerization process can be about 0.90 to 1.0. In someembodiments, the mole fraction of bPL in the inlet to the polymerizationprocess can be from about 0.90 to 1.0. The remainder of the productionstream entering the polymerization process can include secondaryreaction products such as succinic anhydride (in mole fraction of atmost about 0.015, or 0 to 0.015) and left over solvent (e.g., THF) andleftover carbonylation catalyst (in at most about 1000 ppm). In someembodiments, the remainder of the production stream entering thepolymerization process can include carbonylation catalyst components (inat most about 1000 ppm). In some embodiments, the inlet to thepolymerization process can also include a polymerization catalyst, forexample, if the polymerization reaction is a homogenous polymerizationreaction. In some embodiments, the production stream entering thepolymerization process can have a temperature between about 80 to 120°C. In some embodiments, the production stream entering thepolymerization process can be at a pressure of about 0.05 bar to about20 bar.

The system in FIG. 7, the PPL production system/production process isconfigured to operate in a continuous mode, achieving partial conversionof bPL to PPL. The PPL production system/production process may beconfigured to achieve various levels of bPL conversion. For example, insome embodiments, at least 40%, at least 50%, at least 60%, at least70%, at least 80%, or at least 90% of the bPL in the production streamis converted to PPL. In some embodiments, about 50% to about 99% of thebPL in the production stream is converted to PPL. The partialpolymerization stream exits the outlet of the polymerization reactor andenters the inlet of the BPL recycling system. The BPL recycling systemis configured to separate unreacted bPL from the partial polymerizationstream and recycle the bPL back into the polymerization reactor (labeled‘bPL’ in FIG. 7). In some embodiments, the BPL recycling systemcomprises one or more distillation columns, while in other embodimentsthe BPL recycling system comprises one or more wiped-film evaporators(WFE). A PPL product stream (labeled ‘PPL/residual cat.’ in FIG. 7)exits the outlet of the BPL recycling system, and comprises PPL withtrace amount of carbonylation catalyst. In some embodiments, the PPLproduct stream comprises PPL with trace amount of carbonylation catalystcomponents. In some embodiments, the polymerization process can produceabout 2000 kg/hr PPL to about 35000 kg/hr PPL. In some embodiments, thepolymerization process can produce about 25 kmol/hr PPL to about 500kmol/hr PPL.

In some embodiments, the mass fraction of PPL in the PPL product streamcan be about 0.90 to 1.0. In some embodiments, the mole fraction of PPLin the PPL product stream can be about 0.90 to 1.0. The remainder of thePPL product stream can include unreacted bPL (in mole fraction of atmost about 0.02, or 0 to 0.02), secondary reaction products such assuccinic anhydride (in mole fraction of at most about 0.01, or from 0 to0.01) and left over solvent (e.g., THF) and leftover carbonylationcatalyst (in at most about 1000 ppm). In some embodiments, the remainderof the PPL product stream can include carbonylation catalyst components(in at most about 1000 ppm). In some embodiments, the PPL product streamcan have a temperature between about 100° C. to 140° C. In someembodiments, the PPL product stream can be at a pressure of at leastabout 0.001 bar.

The PPL product stream enters the inlet of the PPL purification system(labeled ‘IER’ in FIG. 7). In some variations, the PPL purificationsystem may use an ion exchange resin (IER) to reduce the concentrationof carbonylation catalyst in the PPL product stream. The cationic andanionic carbonylation catalyst species are recovered from the IER in thePPL purification system and can be regenerated to obtain catalystavailable for recycle to the carbonylation reactor or be disposed of(labeled ‘Regenerate/Dispose’ in FIG. 7). A post-purification PPLproduct stream exits an outlet of the PPL purification system and entersan inlet of the thermolysis reactor. The post-purification PPL productstream may have any concentration of compounds, temperature, or pressuredescribed herein. For example, in some embodiments, the mass fraction ofPPL in the post-purification PPL product stream can be about 0.90 to1.0. In some embodiments, the mole fraction of PPL in thepost-purification PPL product stream can be about 0.90 to 1.0. In someembodiments, the post-purification PPL product stream can have atemperature between about 100° C. to about 140° C. In some embodiments,the post-purification PPL product stream can be at a pressure of atleast about 0.001 bar.

The system in FIG. 7, the glacial acrylic acid productionsystem/production process is configured to convert the post-purificationPPL stream to a GAA stream. Traces of high boiling organic impurities(labeled ‘Organic Heavies’ in FIG. 7) are output via an outlet of thethermolysis reactor, and are sent to the incinerator for disposal(labeled ‘Incinerator’ in FIG. 7). A GAA product stream exits an outletof the thermolysis reactor, and may be condensed, further processed orstored. The GAA product stream may exit an outlet of the thermolysisreactor at any rate, concentration, temperature, or pressure describedherein. The remainder of the GAA product stream can include secondaryreaction products such as succinic anhydride and left over solvent suchas THF. In some embodiments, the GAA product stream can have atemperature between about 15° C. to about 60° C. In some embodiments,the GAA product stream can be at a pressure of about 0.5 bar to about1.5 bar.

The exemplary production system/production process depicted in FIG. 7may produce GAA at any rate described herein. For example, in someembodiments, the system produces at least about 25 kilo tons per annum(“KTA”) to about 400 KTA for annual production operation of about 8000hours. In some embodiments, the production system/production process canproduce at least about 2000 kg/hr GAA, or between about 2000 kg/hr GAAand about 35000 kg/hr GAA. In some embodiments, the productionsystem/production process can produce about 25 kmol/hr GAA to about 500kmol/hr GAA.

FIG. 8 depicts an exemplary production system/production process wherethe PPL product stream and the GAA product stream are produced at thesame location, carbonylation catalyst or components thereof are notremoved from the PPL product stream prior to entering the thermolysisreactor, the conversion of bPL to PPL in the polymerization process iscomplete with no recycling of bPL to the polymerization process, andcarbonylation catalyst or components thereof are removed from theorganic heavies produced by the thermolysis reactor. The productionsystem/production process in FIG. 8 has the same configuration ofcarbonylation reactor, CO catalyst recycling, EO/CO recycling and BPLpurification system as shown in FIG. 6.

With reference again to the exemplary system in FIG. 8, the productionstream exits the outlet of the BPL purification system and enters theinlet of the polymerization process. In the production system/productionprocess depicted in FIG. 8, the polymerization process comprises apolymerization reactor (labeled ‘Polymerization’ in FIG. 8). An inlet tothe polymerization process may include any rate, concentration,temperature, or pressure of production stream described herein. Forexample, in one embodiment, the inlet to the polymerization process caninclude about 2000 kg/hr bPL to about 35000 kg/hr bPL. In someembodiments, the inlet to the polymerization process can include about25 kmol/hr bPL to about 500 kmol/hr bPL. In some embodiments, the massfraction of bPL in the inlet to the polymerization process can be about0.90 to 1.0. In some embodiments, the mole fraction of bPL in the inletto the polymerization process can be from about 0.90 to 1.0. Theremainder of the production stream entering the polymerization processcan include secondary reaction products such as succinic anhydride (inmole fraction of at most about 0.015, or 0 to 0.015), leftover solvent(e.g., THF) and leftover carbonylation catalyst (in at most about 1000ppm). In some embodiments, the remainder of the production streamentering the polymerization process can include carbonylation catalystcomponents (in at most about 1000 ppm). In some embodiments, the inletto the polymerization process can also include a polymerizationcatalyst, for example, if the polymerization reaction is a homogenouspolymerization reaction. In some embodiments, the production streamentering the polymerization process can have a temperature between about80° C. to about 120° C. In some embodiments, the production streamentering the polymerization process can be at a pressure of about 0.05bar to about 0.15 bar.

With reference again to the exemplary system in FIG. 8, thepolypropiolactone production system/production process is configured tooperate in a continuous mode, achieving complete conversion of bPL inthe production stream to PPL. A PPL product stream (labeled‘PPL/residual cat.’ in FIG. 8) exits the polymerization process outlet,and comprises PPL with trace amount of carbonylation catalyst. In someembodiments, the PPL product stream comprises PPL with trace amount ofcarbonylation catalyst components.

In some embodiments, the polymerization process can produce about 2000kg/hr PPL to about 35000 kg/hr PPL. In some embodiments, thepolymerization process can produce about 25 kmol/hr PPL to about 500kmol/hr PPL.

In some embodiments, the mass fraction of PPL in the PPL product streamcan be about 0.90 to 1.0. In some embodiments, the mole fraction of PPLin the PPL product stream can be about 0.90 to 1.0. The remainder of thePPL product stream can include unreacted bPL (in mole fraction of atmost about 0.02, or from 0 to 0.02), secondary reaction products such assuccinic anhydride (in mole fraction of at most about 0.01, or from 0 to0.01), leftover solvent (e.g., THF) and leftover carbonylation catalyst(in at most about 1000 ppm). In some embodiments, the PPL product streamcan have a temperature between about 100° C. to about 140° C. In someembodiments, the PPL product stream can be at a pressure of at leastabout 0.001 bar.

With reference again to the exemplary system in FIG. 8, the PPL productstream enters the inlet of the thermolysis reactor. The thermolysisreactor is configured to convert the PPL product stream to a GAA stream.Traces of high boiling organic impurities (labeled ‘Organic Heavies’ inFIG. 8) are output via an outlet of the thermolysis reactor. The streamof high boiling organic impurities enters a purification system (labeled‘IER’ in FIG. 8) comprising ion exchange resin (IER) which may be usedin some embodiments may be useful. The IER is configured to reduce theconcentration of carbonylation catalyst in the stream of high boilingorganic impurities. In some embodiments, the concentration ofcarbonylation catalyst in the stream of high boiling organic impuritiesis between 100 ppm to 1000 ppm before entering the purification system,and is less than 50 ppm, less than 20 ppm, or less than 5 ppm afterexiting the purification system.

The cationic and anionic carbonylation catalyst species are recoveredfrom the IER and can be regenerated to obtain catalyst available forrecycle to the carbonylation reactor or be disposed of (labeled‘Regenerate/Dispose’ in FIG. 8). A GAA product stream exits an outlet ofthe thermolysis reactor for storage or further processing. The GAAproduct stream comprises essentially pure GAA. A GAA product streamexits an outlet of the thermolysis reactor for storage or furtherprocessing. The GAA product stream comprises essentially pure GAA. TheGAA product stream may exit an outlet of the thermolysis reactor at anyrate, concentration, temperature, or pressure described herein. Theremainder of the GAA product stream can include secondary reactionproducts such as succinic anhydride and left over solvent such as THF.In some embodiments, the GAA product stream can have a temperaturebetween about 15° C. to about 60° C. In some embodiments, the GAAproduct stream can be at a pressure of about 0.5 to about 1.5 bar.

The exemplary production system/production process depicted in FIG. 8may produce GAA at any rate described herein. For example, in someembodiments, the system produces at least about 25 kilo tons per annum(“KTA”), or between about 25 KTA to about 400 KTA for annual productionoperation of about 8000 hours. In some embodiments, the productionsystem/production process can produce at least about 2000 kg/hr GAA, orbetween about 2000 kg/hr GAA to about 35000 kg/hr GAA. In someembodiments, the production system/production process can produce about25 kmol/hr GAA to about 500 kmol/hr GAA.

FIG. 9 depicts an exemplary production system/production process wherethe PPL product stream and the GAA product stream are produced at thesame location, carbonylation catalyst or components thereof are notremoved from the PPL product stream prior to entering the thermolysisreactor, the conversion of bPL to PPL in the polymerization process isin complete and bPL is recycled back to the polymerization process, andcarbonylation catalyst or components thereof are removed from theorganic heavies produced by the thermolysis reactor. The productionsystem/production process in FIG. 9 has the same configuration ofcarbonylation reactor, CO catalyst recycling, EO/CO recycling and BPLpurification system as shown in FIG. 6.

With reference again to the exemplary system in FIG. 9, the productionstream comprising purified bPL exits the outlet of the BPL purificationsystem. The production stream contains trace amounts of carbonylationcatalyst, but is essentially free of THF, EO, CO, ACH, and SAH. Theproduction stream is fed forward and enters an inlet of thepolymerization process. The polymerization process comprises apolymerization reactor (labeled ‘Polymerization’ in FIG. 9) and a BPLrecycling system (labeled ‘Distill/WFE’ in FIG. 9). An inlet to thepolymerization process may include any rate, concentration, temperature,or pressure of production stream described herein. For example, in oneembodiment, the inlet to the polymerization process can include about2000 kg/hr bPL to about 35000 kg/hr bPL. In some embodiments, the inletto the polymerization process can include about 25 kmol/hr bPL to about500 kmol/hr bPL. In some embodiments, the mass fraction of bPL in theinlet to the polymerization process can be about 0.90 to 1.0. In someembodiments, the mole fraction of bPL in the inlet to the polymerizationprocess can be from about 0.90 to 1.0. The remainder of the productionstream entering the polymerization process can include secondaryreaction products such as succinic anhydride (in mole fraction of atmost about 0.015, or from 0 to 0.015) and left over solvent (e.g., THF)and leftover carbonylation catalyst (in at most about 1000 ppm). In someembodiments, the inlet to the polymerization process can also include apolymerization catalyst, for example, if the polymerization reaction isa homogenous polymerization reaction. In some embodiments, theproduction stream entering the polymerization process can have atemperature between about 80° C. to 120° C. In some embodiments, theproduction stream entering the polymerization process can be at apressure of about 0.05 bar to about 20 bar.

With reference again to the exemplary system in FIG. 9, thepolypropiolactone production system/production process is configured tooperate in a continuous mode, achieving partial conversion of bPL in theproduction stream to PPL. The polypropiolactone productionsystem/production process may be configured to achieve various levels ofbPL conversion. For example, in some embodiments, at least 40%, at least50%, at least 60%, at least 70%, at least 80%, or at least 90% of thebPL in the production stream is converted to PPL. In some embodiments,about 50% to about 95% of the bPL in the production stream is convertedto PPL. In some embodiments, about 50% to about 99% of the bPL in theproduction stream is converted to PPL. The partial polymerization streamexits the outlet of the polymerization reactor and enters the inlet ofthe BPL recycling system. The BPL recycling system is configured toseparate unreacted bPL from the partial polymerization stream andrecycle the bPL back into the polymerization reactor (labeled ‘bPL’ inFIG. 9). In some embodiments, the BPL recycling system comprises one ormore distillation columns, while in other embodiments the BPL recyclingsystem comprises one or more wiped-film evaporators (WFE). A PPL productstream (labeled ‘PPL/residual cat.’ in FIG. 9) exits the outlet of theBPL recycling system, and comprises PPL with trace amount ofcarbonylation catalyst. In some embodiments, the PPL product streamcomprises PPL with trace amount of carbonylation catalyst components. Insome embodiments, the polymerization process is configured to produceabout 2000 kg/hr PPL to about 35000 kg/hr PPL. In some embodiments, thepolymerization process is configured to produce from about 25 kmol/hrPPL to about 500 kmol/hr PPL.

In some embodiments, the mass fraction of PPL in the PPL product streamcan be about 0.90 to 1.0. In some embodiments, the mole fraction of PPLin the PPL product stream can be about 0.90 to 1.0. The remainder of thePPL product stream can include unreacted bPL (in mole fraction of atmost about 0.02, or from 0 to 0.02), secondary reaction products such assuccinic anhydride (in mole fraction of at most about 0.01, or from 0 to0.01), leftover solvent (e.g., THF) and leftover carbonylation catalyst(in at most about 1000 ppm). In some embodiments, the PPL product streamcan have a temperature between about 100° C. to 140° C. In someembodiments, the PPL product stream can be at a pressure of at leastabout 0.001 bar.

With reference again to the exemplary system in FIG. 9, the PPL productstream enters the inlet of the thermolysis reactor. The thermolysisreactor is configured to convert the PPL product stream to a GAA stream.Traces of high boiling organic impurities (labeled ‘Organic Heavies’ inFIG. 9) are output via an outlet of the thermolysis reactor. The streamof high boiling organic impurities enters a purification system (labeled‘IER’ in FIG. 9) comprising ion exchange resin (IER). The IER isconfigured to reduce the concentration of carbonylation catalyst (orcomponents thereof) in the stream of high boiling organic impurities.The cationic and anionic carbonylation catalyst species are recoveredfrom the IER and can be regenerated to obtain catalyst available forrecycle to the carbonylation reactor or be disposed of (labeled‘Regenerate/Dispose’ in FIG. 9). A GAA product stream exits an outlet ofthe thermolysis reactor for storage or further processing. The GAAproduct stream comprises essentially pure GAA. The GAA product streammay exit an outlet of the thermolysis reactor at any rate,concentration, temperature, or pressure described herein. The remainderof the GAA product stream can include secondary reaction products suchas succinic anhydride and leftover solvent such as THF. In someembodiments, the GAA product stream can have a temperature between about15° C. to about 60° C. In some embodiments, the GAA product stream canbe at a pressure of about 0.5 to about 1.5 bar.

The exemplary production system/production process depicted in FIG. 9may produce GAA at any rate described herein. For example, in someembodiments, the system produces at least about 25 kilo tons per annum(“KTA”), or between about 25 KTA and about 400 KTA for annual productionoperation of about 8000 hours. In some embodiments, the productionsystem/production process can produce at least about 2000 kg/hr GAA, orbetween about 2000 kg/hr GAA and about 35000 kg/hr GAA. In someembodiments, the production system/production process can produce about25 kmol/hr GAA to about 500 kmol/hr GAA.

FIG. 10 depicts another exemplary production system/production processwhere the PPL product stream is produced at a first location, thenisolated, packaged, and shipped to a second location where the GAAproduct stream is produced; carbonylation catalyst or components thereofare removed from the PPL product stream prior to entering thethermolysis reactor, the polymerization reactor achieves completeconversion of bPL in the production stream to PPL and bPL is notrecycled back to the polymerization reactor. The productionsystem/production process in FIG. 10 has the same configuration ofcarbonylation reactor, CO catalyst recycling, EO/CO recycling and BPLpurification system, polymerization process, PPL purification system,and regeneration or disposal of carbonylation catalyst components asshown in FIG. 6.

With reference again to the exemplary system in FIG. 10, thepost-purification PPL product stream exits an outlet of the PPLpurification system and is pelletized, extruded, flaked, powdered, orgranulated by any means known in the art in essentially dry atmosphere.The solid post-purification PPL product stream is then fed forward topackaging, and becomes ready to be shipped to the location of the GAAproduction system/production process. The packaging used to ship thesolid post-purification PPL product stream is selected to minimize themoisture absorption by solid PPL. At the location of the GAA productionsystem/production process, the essentially pure, essentially dry solidpost-purification PPL product stream is unpackaged in a way to minimizeintroduction of moisture, and then fed in a solid or molten form to theinlet of the thermolysis reactor. The thermolysis reactor is configuredto convert the post-isolation PPL product stream to a GAA stream. Tracesof high boiling organic impurities (labeled ‘Organic Heavies’ in FIG.10) are output via an outlet of the thermolysis reactor and sent to anincinerator for disposal (labeled ‘Incinerator’ in FIG. 10). A GAAproduct stream exits an outlet of the thermolysis reactor for storage orfurther processing. The GAA product stream comprises essentially pureGAA. The GAA product stream may exit an outlet of the thermolysisreactor at any rate, concentration, temperature, or pressure describedherein. The remainder of the GAA product stream can include secondaryreaction products such as succinic anhydride and left over solvent suchas THF. In some embodiments, the GAA product stream can have atemperature between about 15° C. to about 60° C. In some embodiments,the GAA product stream can be at a pressure of about 0.5 to about 1.5bar.

The exemplary production system/production process depicted in FIG. 10may produce GAA at any rate described herein. For example, in someembodiments, the system produces at least about 25 kilo tons per annum(“KTA”), or between about 25 KTA and about 400 KTA for annual productionoperation of about 8000 hours. In some embodiments, the productionsystem/production process can produce at least about 2000 kg/hr GAA, orbetween about 2000 kg/hr GAA and about 35000 kg/hr GAA. In someembodiments, the production system/production process can produce about25 kmol/hr GAA to about 500 kmol/hr GAA.

FIG. 11 depicts an exemplary production system/production process wherethe PPL product stream is produced at a first location, then isolated,packaged, and shipped to a second location where the GAA product streamis produced; carbonylation catalyst or components thereof are removedfrom the PPL product stream prior to entering the thermolysis reactor,the polymerization reactor achieves incomplete conversion of bPL in theproduction stream to PPL and bPL is recycled back to the polymerizationreactor. The production system/production process in FIG. 11 has thesame configuration of carbonylation reactor, CO catalyst recycling,EO/CO recycling and BPL purification system, polymerization process, PPLpurification system, and regeneration or disposal of carbonylationcatalyst components as shown in FIG. 7.

With reference again to the exemplary system in FIG. 11, thepost-purification PPL product stream exits an outlet of the PPLpurification system and is pelletized, extruded, flaked, powdered, orgranulated by means known in the art in essentially dry atmosphere. Thesolid post-purification PPL product stream is then fed forward topackaging, and becomes ready to be shipped to the location of the GAAproduction system/production process. The packaging used to ship thesolid post-purification PPL product stream is selected to minimize themoisture absorption by solid PPL. At the location of the GAA productionsystem/production process, the essentially pure, essentially dry solidpost-purification PPL product stream is unpackaged in a way to minimizeintroduction of moisture, and then fed in a solid or molten form to theinlet of the thermolysis reactor. The thermolysis reactor is configuredto convert the post-isolation PPL product stream to a GAA stream. Tracesof high boiling organic impurities (labeled ‘Organic Heavies’ in FIG.11) are output via an outlet of the thermolysis reactor and sent to anincinerator for disposal (labeled ‘Incinerator’ in FIG. 11). A GAAproduct stream exits an outlet of the thermolysis reactor for storage orfurther processing. The GAA product stream comprises essentially pureGAA. The GAA product stream may exit an outlet of the thermolysisreactor at any rate, concentration, temperature, or pressure describedherein. The remainder of the GAA product stream can include secondaryreaction products such as succinic anhydride and left over solvent suchas THF. In some embodiments, the GAA product stream can have atemperature between about 15° C. to about 60° C. In some embodiments,the GAA product stream can be at a pressure of about 0.5 to about 1.5bar.

The exemplary production system/production process depicted in FIG. 11may produce GAA at any rate described herein. For example, in someembodiments, the system produces at least about 25 kilo tons per annum(“KTA”), or between about 25 KTA to about 250 KTA for annual productionoperation of about 8000 hours. In some embodiments, the productionsystem/production process can produce at least about 2000 kg/hr GAA, orbetween about 2000 kg/hr GAA to about 35000 kg/hr GAA. In someembodiments, the production system/production process can produce about25 kmol/hr GAA to about 500 kmol/hr GAA.

FIG. 12 depicts another exemplary production system/production processwhere the PPL product stream is produced at a first location, thenisolated, packaged, and shipped to a second location where the GAAproduct stream is produced; carbonylation catalyst or components thereofare not removed from the PPL product stream prior to entering thethermolysis reactor; the polymerization reactor achieves completeconversion of bPL in the production stream to PPL and bPL is notrecycled back to the polymerization reactor; and carbonylation catalystor components thereof are removed from the organic heavies produced bythe thermolysis reactor. The production system/production process inFIG. 12 has the same configuration of carbonylation reactor, CO catalystrecycling, EO/CO recycling and BPL purification system, andpolymerization process as shown in FIG. 8.

With reference again to the exemplary system in FIG. 12, the PPL productstream exits an outlet of the polymerization process and is pelletized,extruded, flaked, powdered, or granulated by means known in the art inessentially dry atmosphere. The solid PPL product stream is then fedforward to packaging, and becomes ready to be shipped to the location ofthe GAA production system/production process. The packaging used to shipthe solid PPL product stream is selected to minimize the moistureabsorption by solid PPL. At the location of the GAA productionsystem/production process, the essentially pure, essentially dry solidPPL product stream is unpackaged in a way to minimize introduction ofmoisture, and then fed in a solid or molten form to the inlet of thethermolysis reactor. The thermolysis reactor is configured to convertthe PPL product stream to a GAA stream. Traces of high boiling organicimpurities (labeled ‘Organic Heavies’ in FIG. 12) are output via anoutlet of the thermolysis reactor. The stream of high boiling organicimpurities enters a purification system (labeled ‘IER’ in FIG. 12)comprising ion exchange and which is an example of one separation themay be employed. The IER is configured to reduce the concentration ofcarbonylation catalyst (or components thereof) in the stream of highboiling organic impurities. The cationic and anionic carbonylationcatalyst species are recovered from the IER and can be regenerated toobtain catalyst available for recycle to the carbonylation reactor or bedisposed of (labeled ‘Regenerate/Dispose’ in FIG. 12). A GAA productstream exits an outlet of the thermolysis reactor for storage or furtherprocessing. The GAA product stream comprises essentially pure GAA. TheGAA product stream may exit an outlet of the thermolysis reactor at anyrate, concentration, temperature, or pressure described herein. Inpreferred embodiment the temperature is controlled to limit the risk ofautopolymerization of acrylic acid. The remainder of the GAA productstream can include secondary reaction products such as succinicanhydride and left over solvent such as THF. In some embodiments, theGAA product stream can have a temperature between about 15° C. to about60° C. In some embodiments, the GAA product stream can be at a pressureof about 0.5 to about 1.5 bar.

The exemplary production system/production process depicted in FIG. 12may produce GAA at any rate described herein. For example, in someembodiments, the system produces at least about 25 kilo tons per annum(“KTA”), or between about 25 KTA and about 400 KTA for annual productionoperation of about 8000 hours. In some embodiments, the productionsystem/production process can produce at least about 2000 kg/hr GAA, orbetween about 2000 kg/hr GAA to about 35000 kg/hr GAA. In someembodiments, the production system/production process can produce about25 kmol/hr GAA to about 500 kmol/hr GAA.

FIG. 13 depicts an exemplary production system/production process wherethe PPL product stream is produced at a first location, then isolated,packaged, and shipped to a second location where the GAA product streamis produced; carbonylation catalyst or components thereof are notremoved from the PPL product stream prior to entering the thermolysisreactor; the polymerization reactor achieves incomplete conversion ofbPL in the production stream to PPL and bPL is recycled back to thepolymerization reactor; and carbonylation catalyst or components thereofare removed from the organic heavies produced by the thermolysisreactor. The production system/production process in FIG. 13 has thesame configuration of carbonylation reactor, CO catalyst recycling,EO/CO recycling and BPL purification system, and polymerization processas shown in FIG. 9.

With reference again to the exemplary system in FIG. 13, the PPL productstream exits an outlet of the polymerization process and is pelletized,extruded, flaked, powdered, or granulated by means known in the art inessentially dry atmosphere. The solid PPL product stream is then fedforward to packaging, and becomes ready to be shipped to the location ofthe GAA production system/production process. The packaging used to shipthe solid PPL product stream is selected to minimize the moistureabsorption by solid PPL. At the location of the GAA productionsystem/production process, the essentially pure, essentially dry solidPPL product stream is unpackaged in a way to minimize introduction ofmoisture, and then fed in a solid or molten form to the inlet of thethermolysis reactor. The thermolysis reactor is configured to convertthe PPL product stream to a GAA stream. Traces of high boiling organicimpurities (labeled ‘Organic Heavies’ in FIG. 13) are output via anoutlet of the thermolysis reactor. The stream of high boiling organicimpurities enters a purification system (labeled ‘IER’ in FIG. 13)comprising ion exchange resin (IER). The IER is configured to reduce theconcentration of carbonylation catalyst (or components thereof) in thestream of high boiling organic impurities. The cationic and anioniccarbonylation catalyst species are recovered from the IER and can beregenerated to obtain catalyst available for recycle to thecarbonylation reactor or be disposed of (labeled ‘Regenerate/Dispose’ inFIG. 13). A GAA product stream exits an outlet of the thermolysisreactor for storage or further processing. The GAA product streamcomprises essentially pure GAA. The GAA product stream may exit anoutlet of the thermolysis reactor at any rate, concentration,temperature, or pressure described herein. The remainder of the GAAproduct stream can include secondary reaction products such as succinicanhydride and left over solvent such as THF. In some embodiments, theGAA product stream can have a temperature between about 15° C. to about60° C. In some embodiments, the GAA product stream can be at a pressureof about 0.5 to about 1.5 bar.

The exemplary production system/production process depicted in FIG. 13may produce GAA at any rate described herein. For example, in someembodiments, the system produces at least about 25 kilo tons per annum(“KTA”), at least about 100 KTA, at least about 110 KTA, at least about120 KTA, at least about 130 KTA, at least about 140 KTA, at least about150 KTA, at least about 160 KTA, at least about 170 KTA, at least about180 KTA, at least about 190 KTA, at least about 200 KTA, at least about250 KTA, at least about 300 KTA, at least about 350 KTA, at least about400 KTA, and in some variations that may be combined with any of thepreceding variations, up to about 400 KTA, for annual productionoperation of about 8000 hours. In some embodiments, the productionsystem/production process can produce at least about 2000 kg/hr GAA, orbetween about 2000 kg/hr GAA and about 35000 kg/hr GAA. In someembodiments, the production system/production process can produce about25 kmol/hr GAA to about 500 kmol/hr GAA.

FIGS. 6-13 depict process configurations comprising certain steps andunit operations, in other embodiments of the methods described hereinthe process configuration contains fewer steps, more steps, fewer unitoperations, or more unit operations. For example, in some variations,the permeate stream is treated to remove at least a portion of the tracecarbonylation catalyst prior to the BPL purification train. In certainvariations, it may be possible to remove of at least a portion of thetrace carbonylation catalyst from the permeate with an ion exchangeresin. Thus, in certain embodiments, the process configurations in FIGS.6-13 includes the additional step of removing at least a portion of thetrace carbonylation catalyst from the permeate using IER, before thepermeate enters the BPL purification train. In some embodiments, thesystems depicted in FIGS. 6-13 and described herein include apurification system with IER before prior to the BPL purification train.In other embodiments, the systems include a purification system with IERprior to the BPL purification train and use a heterogeneouspolymerization catalyst in the polymerization process. In someembodiments, the systems do not have a purification system after thepolymerization process.

Each of the unit operations in the production system/production processfor acrylic acid and precursors thereof are described in further detailbelow.

β-Propiolactone Production System/Production Process (i.e.,Carbonylation Reaction System)

FIG. 14 illustrates an exemplary embodiment of the productionsystem/production process disclosed herein. FIG. 14 containscarbonylation reaction system 1413 (i.e., β-propiolactone productionsystem/production process), catalyst isolation system 1415, BPLpurification system 1417, polymerization reaction system 1419, andthermolysis system 1421.

In the carbonylation reaction system, Ethylene oxide can be converted toβ-propiolactone by a carbonylation reaction, as depicted in the reactionscheme below.

Water and oxygen can damage the carbonylation catalyst. The feed streams(i.e., EO, CO, solvent, carbonylation catalyst) to the carbonylationreaction system should be substantially dry (i.e., have a water contentbelow 5 ppm) and be oxygen free (i.e., have an oxygen content below 5ppm). As such, the feed streams and/or storage tanks and/or feed tankcan have sensors on them in order to determine the composition of thestream/tank to make sure that they have a low enough oxygen and watercontent. In some embodiments, the feed streams can be purified such asby adsorption to reduce the water and oxygen content in the streams fedto the carbonylation reaction system. In some embodiments, prior torunning the production system/production process, the tubes,apparatuses, and other flow paths can be purged with an inert gas orcarbon monoxide to minimize exposure to oxygen or water in theproduction system/production process.

Ethylene Oxide Source

FIG. 14 includes ethylene oxide source 1402 that can feed fresh ethyleneoxide in ethylene oxide stream 1406 to carbonylation reaction systeminlet 1409. Inlet 1409 can be one inlet to the carbonylation reactionsystem or multiple inlets. Ethylene oxide can be fed as a liquid using apump or any other means known to those of ordinary skill in the art. Inaddition, the ethylene oxide source can be maintained under an inertatmosphere. In some embodiments, the inlet to the carbonylation reactionsystem can receive ethylene oxide from an ethylene oxide source at leastabout 1000 kg/hr, at least about 1500 kg/hr, at least about 2000 kg/hr,at least about 2070 kg/hr, or at least about 2500 kg/hr. In someembodiments, the inlet to the carbonylation reaction system can receiveethylene oxide from an ethylene oxide source at about 1000 kg/hr toabout 2500 kg/hr, at least about 1500 kg/hr to about 2500 kg/hr, atleast about 2000 kg/hr to about 2500 kg/hr, or at least about 2070 kg/hrto about 2500 kg/hr. In some embodiments, the inlet to the carbonylationreaction system can receive ethylene oxide from an ethylene oxide sourcefrom about 1000 kg/hr to about 25000 kg/hr, about 1500 kg/hr to about25000 kg/hr, about 2000 kg/hr to about 25000 kg/hr, about 2500 kg/hr toabout 25000 kg/hr, about 5000 kg/hr to about 25000 kg/hr, about 7500kg/hr to about 25000 kg/hr, about 10000 kg/hr to about 25000 kg/hr,about 12500 kg/hr to about 25000 kg/hr, about 15000 kg/hr to about 25000kg/hr, about 17500 kg/hr to about 25000 kg/hr, about 20000 kg/hr toabout 25000 kg/hr, or about 22500 kg/hr to about 25000 kg/hr. In someembodiments, the inlet to the carbonylation reaction system can receiveethylene oxide from an ethylene oxide source at about 1000 kg/hr, about1500 kg/hr, about 2000 kg/hr, about 2070 kg/hr, about 2500 kg/hr, about3000 kg/hr, about 3500 kg/hr, about 4000 kg/hr, about 4500 kg/hr, about5000 kg/hr, 7500 kg/hr, about 10000 kg/hr, about 12500 kg/hr, about15000 kg/hr, about 17500 kg/hr, about 20000 kg/hr, about 22500 kg/hr, orabout 25000 kg/hr. In some embodiments, the inlet to the carbonylationreaction system can receive ethylene oxide from an ethylene oxide sourceat least about 30 kmol/hr, at least about 35 kmol/hr, at least about 40kmol/hr, at least about 47 kmol/hr, at least about 50 kmol/hr, at leastabout 100 kmol/hr, at least about 200 kmol/hr, at least about 300kmol/hr, at least about 400 kmol/hr, or at least about 500 kmol/hr. Insome embodiments, the inlet to the carbonylation reaction system canreceive ethylene oxide from an ethylene oxide source at about 30 kmol/hrto about 500 kmol/hr, about 35 kmol/hr to about 500 kmol/hr, about 40kmol/hr to about 500 kmol/hr, about 47 kmol/hr to about 500 kmol/hr,about 50 kmol/hr to about 500 kmol/hr, about 100 kmol/hr to about 500kmol/hr, about 200 kmol/hr to about 500 kmol/hr, about 300 kmol/hr toabout 500 kmol/hr, or about 400 kmol/hr to about 500 kmol/hr. In someembodiments, the inlet to the carbonylation reaction system can receiveethylene oxide from an ethylene oxide source at about 30 kmol/hr, about35 kmol/hr, about 40 kmol/hr, about 47 kmol/hr, about 50 kmol/hr, about70 kmol/hr, about 80 kmol/hr about 90 kmol/hr, about 100 kmol/hr, about150 kmol/hr, about 200 kmol/hr, about 250 kmol/hr, about 300 kmol/hr,about 350 kmol/hr, about 400 kmol/hr, about 450 kmol/hr, or about 500kmol/hr. In some embodiments, the inlet to the carbonylation reactionsystem can receive ethylene oxide from an ethylene oxide source at atemperature between about 10-30° C., between about 15-25° C., or about20° C. In some embodiments, the inlet to the carbonylation reactionsystem can receive ethylene oxide from an ethylene oxide source at apressure of at least about 50 bar, about 60-70 bar, or at least about 65bar.

Carbonylation Catalyst Source

Numerous carbonylation catalysts known in the art are suitable for (orcan be adapted to) methods of the present invention. For example, insome embodiments, the carbonylation methods utilize a metalcarbonyl-Lewis acid catalyst such as those described in U.S. Pat. No.6,852,865. In other embodiments, the carbonylation step is performedwith one or more of the carbonylation catalysts disclosed in U.S. patentapplication Ser. Nos. 10/820,958; and 10/586,826. In other embodiments,the carbonylation step is performed with one or more of the catalystsdisclosed in U.S. Pat. Nos. 5,310,948; 7,420,064; and 5,359,081.Additional catalysts for the carbonylation of epoxides are discussed ina review in Chem. Commun., 2007, 657-674. The entirety of each of thepreceding references is incorporated herein by reference.

In some embodiments, the carbonylation catalyst includes a metalcarbonyl compound. Typically, a single metal carbonyl compound isprovided, but in some embodiments, mixtures of two or more metalcarbonyl compounds are provided. Thus, when a provided metal carbonylcompound “comprises”, e.g., a neutral metal carbonyl compound, it isunderstood that the provided metal carbonyl compound can be a singleneutral metal carbonyl compound, or a neutral metal carbonyl compound incombination with one or more metal carbonyl compounds. Preferably, theprovided metal carbonyl compound is capable of ring-opening an epoxideand facilitating the insertion of CO into the resulting metal carbonbond. Metal carbonyl compounds with this reactivity are well known inthe art and are used for laboratory experimentation as well as inindustrial processes such as hydroformylation.

In some embodiments, a provided metal carbonyl compound comprises ananionic metal carbonyl moiety. In other embodiments, a provided metalcarbonyl compound comprises a neutral metal carbonyl compound. In someembodiments, a provided metal carbonyl compound comprises a metalcarbonyl hydride or a hydrido metal carbonyl compound. In someembodiments, a provided metal carbonyl compound acts as a pre-catalystwhich reacts in situ with one or more reaction components to provide anactive species different from the compound initially provided. Suchpre-catalysts are specifically encompassed as it is recognized that theactive species in a given reaction may not be known with certainty; thusthe identification of such a reactive species in situ does not itselfdepart from the spirit or teachings of the present disclosure.

In some embodiments, the metal carbonyl compound comprises an anionicmetal carbonyl species. In some embodiments, such anionic metal carbonylspecies have the general formula [Q_(d)M′_(e)(CO)_(w)]^(y−), where Q isany ligand and need not be present, M′ is a metal atom, d is an integerbetween 0 and 8 inclusive, e is an integer between 1 and 6 inclusive, wis a number such as to provide the stable anionic metal carbonylcomplex, and y is the charge of the anionic metal carbonyl species. Insome embodiments, the anionic metal carbonyl has the general formula[QM′(CO)_(w)]^(y−), where Q is any ligand and need not be present, M′ isa metal atom, w is a number such as to provide the stable anionic metalcarbonyl, and y is the charge of the anionic metal carbonyl.

In some embodiments, the anionic metal carbonyl species includemonoanionic carbonyl complexes of metals from groups 5, 7 or 9 of theperiodic table or dianionic carbonyl complexes of metals from groups 4or 8 of the periodic table. In some embodiments, the anionic metalcarbonyl compound contains cobalt or manganese. In some embodiments, theanionic metal carbonyl compound contains rhodium. Suitable anionic metalcarbonyl compounds include, but are not limited to: [Co(CO)₄]⁻,[Ti(CO)₆]²⁻ [V(CO)₆]⁻ [Rh(CO)₄]⁻, [Fe(CO)₄]²⁻ [Ru(CO)₄]²⁻, [Os(CO)₄]²⁻[Cr₂(CO)₁₀]²⁻ [Fe₂(CO)₈]²⁻ [Tc(CO)₅]⁻ [Re(CO)₅]⁻ and [Mn(CO)₅]⁻. In someembodiments, the anionic metal carbonyl comprises [Co(CO)₄]⁻. In someembodiments, a mixture of two or more anionic metal carbonyl complexesmay be present in the carbonylation catalysts used in the methods.

The term “such as to provide a stable anionic metal carbonyl” for[Q_(d)M′_(e)(CO)_(w)]^(y−) is used herein to mean that[Q_(a)M′_(e)(CO)_(w)]^(y−) is a species characterizable by analyticalmeans, e.g., NMR, IR, X-ray crystallography, Raman spectroscopy and/orelectron spin resonance (EPR) and isolable in catalyst form in thepresence of a suitable cation or a species formed in situ. It is to beunderstood that metals which can form stable metal carbonyl complexeshave known coordinative capacities and propensities to form polynuclearcomplexes which, together with the number and character of optionalligands Q that may be present and the charge on the complex willdetermine the number of sites available for CO to coordinate andtherefore the value of w. Typically, such compounds conform to the“18-electron rule”. Such knowledge is within the grasp of one havingordinary skill in the arts pertaining to the synthesis andcharacterization of metal carbonyl compounds.

In embodiments where the provided metal carbonyl compound is an anionicspecies, one or more cations must also necessarily be present. In somevariations, no particular constraints on the identity of such cations.In some embodiments, the cation associated with an anionic metalcarbonyl compound comprises a reaction component of another categorydescribed herein. For example, in some embodiments, the metal carbonylanion is associated with a cationic Lewis acid. In other embodiments acation associated with a provided anionic metal carbonyl compound is asimple metal cation such as those from Groups 1 or 2 of the periodictable (e.g., Na⁺, Li⁺, K⁺, Mg²⁺ and the like). In other embodiments acation associated with a provided anionic metal carbonyl compound is abulky non electrophilic cation such as an ‘onium salt’ (e.g., Bu₄N⁺,PPN⁺, Ph₄P⁺Ph₄As⁺, and the like). In other embodiments, a metal carbonylanion is associated with a protonated nitrogen compound (e.g., a cationmay comprise a compound such as MeTBD-H⁺, DMAP-H⁺, DABCO-H⁺, DBU-H⁺ andthe like). In some embodiments, compounds comprising such protonatednitrogen compounds are provided as the reaction product between anacidic hydrido metal carbonyl compound and a basic nitrogen-containingcompound (e.g., a mixture of DBU and HCo(CO)₄).

In some embodiments, a catalyst utilized in the methods described hereincomprises a neutral metal carbonyl compound. In some embodiments, suchneutral metal carbonyl compounds have the general formulaQ_(d)M′_(e)(CO)_(w′), where Q is any ligand and need not be present, M′is a metal atom, d is an integer between 0 and 8 inclusive, e is aninteger between 1 and 6 inclusive, and w′ is a number such as to providethe stable neutral metal carbonyl complex. In some embodiments, theneutral metal carbonyl has the general formula QM′(CO)_(w′). In someembodiments, the neutral metal carbonyl has the general formulaM′(CO)_(w′). In some embodiments, the neutral metal carbonyl has thegeneral formula QM′₂(CO)_(w′). In some embodiments, the neutral metalcarbonyl has the general formula M′Z₂(CO)_(w′). Suitable neutral metalcarbonyl compounds include, but are not limited to: Ti(CO)₇; V₂(CO)₁₂;Cr(CO)₆; Mo(CO)₆; W(CO)₆Mn₂(CO)₁₀, Tc₂(CO)₁₀, and Re₂(CO)₁₀ Fe(CO)₅,Ru(CO)₅ and Os(CO)₅ Ru₃(CO)₁₂, and Os₃(CO)₁₂Fe₃(CO)₁₂ and Fe₂(CO)₉Co₄(CO)₁₂, Rh₄(CO)₁₂, Rh₆(CO)₁₆, and Ir₄(CO)₁₂ CO₂(CO)₅ Ni(CO)₄.

The term “such as to provide a stable neutral metal carbonyl” forQ_(a)M′_(e)(CO)_(w′) is used herein to mean that Q₀M′_(e)(CO)_(w′) is aspecies characterizable by analytical means, e.g., NMR, IR, X-raycrystallography, Raman spectroscopy and/or electron spin resonance (EPR)and isolable in pure form or a species formed in situ. It is to beunderstood that metals which can form stable metal carbonyl complexeshave known coordinative capacities and propensities to form polynuclearcomplexes which, together with the number and character of optionalligands Q that may be present will determine the number of sitesavailable for CO to coordinate and therefore the value of w′. Typically,such compounds conform to stoichiometries conforming to the “18-electronrule”. Such knowledge is within the grasp of one having ordinary skillin the arts pertaining to the synthesis and characterization of metalcarbonyl compounds.

In some embodiments, no ligands Q are present on the metal carbonylcompound. In other embodiments, one or more ligands Q are present on themetal carbonyl compound. In some embodiments, where Q is present, eachoccurrence of Q is selected from the group consisting of phosphineligands, amine ligands, cyclopentadienyl ligands, heterocyclic ligands,nitriles, phenols, and combinations of two or more of these. In someembodiments, one or more of the CO ligands of any of the metal carbonylcompounds described above is replaced with a ligand Q. In someembodiments, Q is a phosphine ligand. In some embodiments, Q is atriaryl phosphine. In some embodiments, Q is trialkyl phosphine. In someembodiments, Q is a phosphite ligand. In some embodiments, Q is anoptionally substituted cyclopentadienyl ligand. In some embodiments, Qis cp. In some embodiments, Q is cp*. In some embodiments, Q is an amineor a heterocycle.

In some embodiments, the carbonylation catalyst utilized in the methodsdescribed above further includes a Lewis acidic component. In someembodiments, the carbonylation catalyst includes an anionic metalcarbonyl complex and a cationic Lewis acidic component. In someembodiments, the metal carbonyl complex includes a carbonyl cobaltateand the Lewis acidic co-catalyst includes a metal-centered cationicLewis acid. In some embodiments, an included Lewis acid comprises aboron compound.

In some embodiments, where an included Lewis acid comprises a boroncompound, the boron compound comprises a trialkyl boron compound or atriaryl boron compound. In some embodiments, an included boron compoundcomprises one or more boron-halogen bonds. In some embodiments, where anincluded boron compound comprises one or more boron-halogen bonds, thecompound is a dialkyl halo boron compound (e.g., R₂BX), a dihalomonoalkyl compound (e.g., RBX₂), an aryl halo boron compound (e.g.,Ar₂BX or ArBX₂), or a trihalo boron compound (e.g., BCl₃ or BBr₃),wherein each R is an alkyl group; each X is a halogen; and each Ar is anaromatic group.

In some embodiments, where the included Lewis acid comprises ametal-centered cationic Lewis acid, the Lewis acid is a cationic metalcomplex. In some embodiments, the cationic metal complex has its chargebalanced either in part, or wholly by one or more anionic metal carbonylmoieties. Suitable anionic metal carbonyl compounds include thosedescribed above. In some embodiments, there are 1 to 17 such anionicmetal carbonyls balancing the charge of the metal complex. In someembodiments, there are 1 to 9 such anionic metal carbonyls balancing thecharge of the metal complex. In some embodiments, there are 1 to 5 suchanionic metal carbonyls balancing the charge of the metal complex. Insome embodiments, there are 1 to 3 such anionic metal carbonylsbalancing the charge of the metal complex.

In some embodiments, where carbonylation catalysts used in systems andmethods described herein include a cationic metal complex, the metalcomplex has the formula [(L^(c))_(v)M_(b)]^(z+), where:

L^(c) is a ligand where, when two or more LC are present, each may bethe same or different;

M is a metal atom where, when two M are present, each may be the same ordifferent;

v is an integer from 1 to 4 inclusive;

b is an integer from 1 to 2 inclusive; and

z is an integer greater than 0 that represents the cationic charge onthe metal complex.

In some embodiments, provided Lewis acids conform to structure I:

wherein:

is a multidentate ligand;

M is a metal atom coordinated to the multidentate ligand;

a is the charge of the metal atom and ranges from 0 to 2; and

In some embodiments, provided metal complexes conform to structure II:

Where a is as defined above (each a may be the same or different), and

M¹ is a first metal atom;

M² is a second metal atom;

comprises a multidentate ligand system capable of coordinating bothmetal atoms.

For sake of clarity, and to avoid confusion between the net and totalcharge of the metal atoms in complexes I and II and other structuresherein, the charge (a⁺) shown on the metal atom in complexes I and IIabove represents the net charge on the metal atom after it has satisfiedany anionic sites of the multidentate ligand. For example, if a metalatom in a complex of formula I were Cr(III), and the ligand wereporphyrin (a tetradentate ligand with a charge of −2), then the chromiumatom would have a net charge of +1, and a would be 1.

Suitable multidentate ligands include, but are not limited to: porphyrinderivatives 1, salen derivatives 2,dibenzotetramethyltetraaza[14]annulene (tmtaa) derivatives 3,derivatives 4, derivatives of the Trost ligand 5, tetraphenylporphyrinderivatives 6, and corrole derivatives 7. In some embodiments, themultidentate ligand is a salen derivative. In other embodiments, themultidentate ligand is a porphyrin derivative. In other embodiments, themultidentate ligand is a tetraphenylporphyrin derivative. In otherembodiments, the multidentate ligand is a corrole derivative.

where each of R^(c), R^(d), R^(1a), R^(2a), R^(3a), R^(4a), R^(1a′),R^(2a′), R^(3a′), and M, is as defined and described in the classes andsubclasses herein.

In some embodiments, Lewis acids provided carbonylation catalysts usedin systems and methods described herein comprise metal-porphinatocomplexes. In some embodiments, the moiety

has the structure:

where each of M and a is as defined above and described in the classesand subclasses herein, and

-   -   R^(d) at each occurrence is independently hydrogen, halogen,        —OR⁴, —NR^(y) ₂, —SR^(y), —CN, —NO₂, —SO₂R^(y), —SOR^(y),        —SO₂NR^(y) ₂; —CNO, —NR^(y)SO₂R^(y), —NCO, —N₃, —SiR^(y) ₃; or        an optionally substituted group selected from the group        consisting of C₁₋₂₀ aliphatic; C₁₋₂₀ heteroaliphatic having 1-4        heteroatoms independently selected from the group consisting of        nitrogen, oxygen, and sulfur; 6- to 10-membered aryl; 5- to        10-membered heteroaryl having 1-4 heteroatoms independently        selected from nitrogen, oxygen, and sulfur; and 4- to 7-membered        heterocyclic having 1-2 heteroatoms independently selected from        the group consisting of nitrogen, oxygen, and sulfur, where two        or more R^(d) groups may be taken together to form one or more        optionally substituted rings,    -   each R^(y) is independently hydrogen, an optionally substituted        group selected the group consisting of acyl; carbamoyl,        arylalkyl; 6- to 10-membered aryl; C₁₋₁₂ aliphatic; C₁₋₁₂        heteroaliphatic having 1-2 heteroatoms independently selected        from the group consisting of nitrogen, oxygen, and sulfur; 5- to        10-membered heteroaryl having 1-4 heteroatoms independently        selected from the group consisting of nitrogen, oxygen, and        sulfur; 4- to 7-membered heterocyclic having 1-2 heteroatoms        independently selected from the group consisting of nitrogen,        oxygen, and sulfur; an oxygen protecting group; and a nitrogen        protecting group; two R^(y) on the same nitrogen atom are taken        with the nitrogen atom to form an optionally substituted 4- to        7-membered heterocyclic ring having 0-2 additional heteroatoms        independently selected from the group consisting of nitrogen,        oxygen, and sulfur; and    -   each R⁴ is independently is a hydroxyl protecting group or        R^(y).

In some embodiments, the moiety

has the structure:

where M, a and R^(d) are as defined above and in the classes andsubclasses herein.

In some embodiments, the moiety

has the structure:

where M, a and R^(d) are as defined above and in the classes andsubclasses herein.

In some embodiments, Lewis acids included in carbonylation catalystsused in systems and methods described herein comprise metallo salenatecomplexes. In some embodiments, the moiety

has the structure:

wherein:

-   -   M, and a are as defined above and in the classes and subclasses        herein.    -   R^(1a), R^(1a′), R^(2a), R^(2a′), R^(3a), and R^(3a′) are        independently hydrogen, halogen, —OR⁴, —NR^(y) ₂, —R^(y)W, —CN,        —NO₂, —SO₂R^(y), —SOR^(y), —SO₂NR^(y) ₂; —CNO, —NR^(y)SO₂R^(y),        —NCO, —N₃, —SiR^(y) ₃; or an optionally substituted group        selected from the group consisting of C₁₋₂₀ aliphatic; C₁₋₂₀        heteroaliphatic having 1-4 heteroatoms independently selected        from the group consisting of nitrogen, oxygen, and sulfur; 6- to        10-membered aryl; 5- to 10-membered heteroaryl having 1-4        heteroatoms independently selected from nitrogen, oxygen, and        sulfur; and 4- to 7-membered heterocyclic having 1-2 heteroatoms        independently selected from the group consisting of nitrogen,        oxygen, and sulfur; wherein each R⁴, and R^(y) is independently        as defined above and described in classes and subclasses herein,    -   wherein any of (R^(2a′) and R^(3a′)), (R^(2a) and R^(3a)),        (R^(1a) and R^(2a)), and (R^(1a′) and R^(2a′)) may optionally be        taken together with the carbon atoms to which they are attached        to form one or more rings which may in turn be substituted with        one or more R^(y) groups; and    -   R^(4a) is selected from the group consisting of:

where

-   -   R^(c) at each occurrence is independently hydrogen, halogen,        —OR⁴, —NR^(y) ₂, —SR^(y), —CN, —NO₂, —SO₂R^(y), —SOR^(y),        —SO₂NR^(y) ₂; —CNO, —NR^(y)SO₂R^(y), —NCO, —N₃, —SiR^(y) ₃; or        an optionally substituted group selected from the group        consisting of C₁₋₂₀ aliphatic; C₁₋₂₀ heteroaliphatic having 1-4        heteroatoms independently selected from the group consisting of        nitrogen, oxygen, and sulfur; 6- to 10-membered aryl; 5- to        10-membered heteroaryl having 1-4 heteroatoms independently        selected from nitrogen, oxygen, and sulfur; and 4- to 7-membered        heterocyclic having 1-2 heteroatoms independently selected from        the group consisting of nitrogen, oxygen, and sulfur;    -   where:        -   two or more R^(c) groups may be taken together with the            carbon atoms to which they are attached and any intervening            atoms to form one or more rings;        -   when two R^(c) groups are attached to the same carbon atom,            they may be taken together along with the carbon atom to            which they are attached to form a moiety selected from the            group consisting of: a 3- to 8-membered spirocyclic ring, a            carbonyl, an oxime, a hydrazone, an imine; and an optionally            substituted alkene;    -   where R⁴ and R^(y) are as defined above and in classes and        subclasses herein;    -   Y is a divalent linker selected from the group consisting of:        —NR^(y)—, —N(R^(y))C(O)—, —C(O)NR^(y)—, —O—, —C(O)—, —OC(O)—,        —C(O)O—, —S—, —SO—, —SO₂—, —C(═S)—, —C(═NR^(y))—, —N═N—; a        polyether; a C₃ to C₈ substituted or unsubstituted carbocycle;        and a C₁ to C₈ substituted or unsubstituted heterocycle;    -   m′ is 0 or an integer from 1 to 4, inclusive;    -   q is 0 or an integer from 1 to 4, inclusive; and    -   x is 0, 1, or 2.

In some embodiments, a provided Lewis acid comprises a metallo salencompound, as shown in formula Ia:

-   -   wherein each of M, R^(d), and a, is as defined above and in the        classes and subclasses herein,        represents is an optionally substituted moiety linking the two        nitrogen atoms of the diamine portion of the salen ligand, where        is selected from the group consisting of a C₃-C₁₄ carbocycle, a        C₆-C₁₀ aryl group, a C₃-C₁₄ heterocycle, and a C₅-C₁₀ heteroaryl        group; or an optionally substituted C₂₋₂₀ aliphatic group,        wherein one or more methylene units are optionally and        independently replaced by —NR^(y)—, —N(R^(y))C(O)—,        —C(O)N(R^(y))—, —OC(O)N(R^(y))—, —N(R^(y))C(O)O—, —OC(O)O—, —O—,        —C(O)—, —OC(O)—, —C(O)O—, —S—, —SO—, —SO₂—, —C(═S)—,        —C(═NR^(y))—, —C(═NR^(y))— or —N═N—.

In some embodiments metal complexes having formula Ia above, at leastone of the phenyl rings comprising the salicylaldehyde-derived portionof the metal complex is independently selected from the group consistingof:

In some embodiments, a provided Lewis acid comprises a metallo salencompound, conforming to one of formulae Va or Vb:

-   -   where M, a, R^(d), R^(1a), R^(3a), R^(1a′), R^(3a′), and        are as defined above and in the classes and subclasses herein.

In some embodiments of metal complexes having formulae Va or Vb, eachR^(1a) and R^(3a) is, independently, optionally substituted C₁-C₂₀aliphatic.

In some embodiments, the moiety

comprises an optionally substituted 1,2-phenyl moiety.

In some embodiments, Lewis acids included in carbonylation catalystsused in systems and methods described herein comprise metal-tmtaacomplexes. In some embodiments, the moiety

has the structure:

where M, a and R^(d) are as defined above and in the classes andsubclasses herein, and

-   R^(e) at each occurrence is independently hydrogen, halogen, —OR,    —NR^(y) ₂, —SR^(y), —CN, —NO₂, —SO₂R^(y), —SOR^(y), —SO₂NR^(y) ₂;    —CNO, —NR^(y)SO₂R^(y), —NCO, —N₃, —SiR^(y) ₃; or an optionally    substituted group selected from the group consisting of C₁₋₂₀    aliphatic; C₁₋₂₀ heteroaliphatic having 1-4 heteroatoms    independently selected from the group consisting of nitrogen,    oxygen, and sulfur; 6- to 10-membered aryl; 5- to 10-membered    heteroaryl having 1-4 heteroatoms independently selected from    nitrogen, oxygen, and sulfur; and 4- to 7-membered heterocyclic    having 1-2 heteroatoms independently selected from the group    consisting of nitrogen, oxygen, and sulfur.

In some embodiments, the moiety

has the structure:

where each of M, a, R^(c) and R^(d) is as defined above and in theclasses and subclasses herein.

In some embodiments, where carbonylation catalysts used in systems andmethods described herein include a Lewis acidic metal complex, the metalatom is selected from the periodic table groups 2-13, inclusive. In someembodiments, M is a transition metal selected from the periodic tablegroups 4, 6, 11, 12 and 13. In some embodiments, M is aluminum,chromium, titanium, indium, gallium, zinc cobalt, or copper. In someembodiments, M is aluminum. In other embodiments, M is chromium.

In some embodiments, M has an oxidation state of +2. In someembodiments, M is Zn(II), Cu(II), Mn(II), Co(II), Ru(II), Fe(II),Co(II), Rh(II), Ni(II), Pd(II) or Mg(II). In some embodiments M isZn(II). In some embodiments M is Cu(II).

In some embodiments, M has an oxidation state of +3. In someembodiments, M is Al(III), Cr(III), Fe(III), Co(III), Ti(III) In(III),Ga(III) or Mn(III). In some embodiments M is Al(III). In someembodiments M is Cr(III).

In some embodiments, M has an oxidation state of +4. In someembodiments, M is Ti(IV) or Cr(IV).

In some embodiments, M¹ and M² are each independently a metal atomselected from the periodic table groups 2-13, inclusive. In someembodiments, M is a transition metal selected from the periodic tablegroups 4, 6, 11, 12 and 13. In some embodiments, M is aluminum,chromium, titanium, indium, gallium, zinc cobalt, or copper. In someembodiments, M is aluminum. In other embodiments, M is chromium. In someembodiments, M¹ and M² are the same. In some embodiments, M¹ and M² arethe same metal, but have different oxidation states. In someembodiments, M¹ and M² are different metals.

In some embodiments, one or more of M¹ and M² has an oxidation state of+2. In some embodiments, M¹ is Zn(II), Cu(II), Mn(II), Co(II), Ru(II),Fe(II), Co(II), Rh(II), Ni(II), Pd(II) or Mg(II). In some embodiments M¹is Zn(II). In some embodiments M¹ is Cu(II). In some embodiments, M² isZn(II), Cu(II), Mn(II), Co(II), Ru(II), Fe(II), Co(II), Rh(II), Ni(II),Pd(II) or Mg(II). In some embodiments M² is Zn(II). In some embodimentsM² is Cu(II).

In some embodiments, one or more of M¹ and M² has an oxidation state of+3. In some embodiments, M¹ is Al(III), Cr(III), Fe(III), Co(III),Ti(III) In(III), Ga(III) or Mn(III). In some embodiments M¹ is Al(III).In some embodiments M¹ is Cr(III). In some embodiments, M² is Al(III),Cr(III), Fe(III), Co(III), Ti(III) In(III), Ga(III) or Mn(III). In someembodiments M² is Al(III). In some embodiments M² is Cr(III).

In some embodiments, one or more of M¹ and M² has an oxidation state of+4. In some embodiments, M′ is Ti(IV) or Cr(IV). In some embodiments, M²is Ti(IV) or Cr(IV).

In some embodiments, the metal-centered Lewis-acidic component of thecarbonylation catalyst includes a dianionic tetradentate ligand. In someembodiments, the dianionic tetradentate ligand is selected from thegroup consisting of: porphyrin derivatives; salen derivatives;dibenzotetramethyltetraaza[14]annulene (tmtaa) derivatives;phthalocyaninate derivatives; and derivatives of the Trost ligand.

In some embodiments, the carbonylation catalyst includes a carbonylcobaltate in combination with an aluminum porphyrin compound. In someembodiments, the carbonylation catalyst is [(TPP)Al(THF)₂][Co(CO)₄]where TPP stands for tetraphenylporphyrin and THF stands fortetrahydrofuran.

In some embodiments, the carbonylation catalyst includes a carbonylcobaltate in combination with a chromium porphyrin compound.

In some embodiments, the carbonylation catalyst includes a carbonylcobaltate in combination with a chromium salen compound. In someembodiments, the carbonylation catalyst includes a carbonyl cobaltate incombination with a chromium salophen compound.

In some embodiments, the carbonylation catalyst includes a carbonylcobaltate in combination with an aluminum salen compound. In someembodiments, the carbonylation catalyst includes a carbonyl cobaltate incombination with an aluminum salophen compound.

In some embodiments, one or more neutral two electron donors coordinateto M M¹ or M² and fill the coordination valence of the metal atom. Insome embodiments, the neutral two electron donor is a solvent molecule.In some embodiments, the neutral two electron donor is an ether. In someembodiments, the neutral two electron donor is tetrahydrofuran, diethylether, acetonitrile, carbon disulfide, or pyridine. In some embodiments,the neutral two electron donor is tetrahydrofuran. In some embodiments,the neutral two electron donor is an epoxide. In some embodiments, theneutral two electron donor is an ester or a lactone.

In certain embodiments, the carbonylation catalyst includes a carbonylcobaltate in combination with an aluminum porphyrin compound. In certainembodiments, the carbonylation catalyst includes a carbonyl cobaltate incombination with a chromium porphyrin compound. In certain embodiments,the carbonylation catalyst includes a carbonyl cobaltate in combinationwith a chromium salen compound. In certain embodiments, thecarbonylation catalyst includes a carbonyl cobaltate in combination witha chromium salophen compound. In certain embodiments, the carbonylationcatalyst includes a carbonyl cobaltate in combination with an aluminumsalen compound. In certain embodiments, the carbonylation catalystincludes a carbonyl cobaltate in combination with an aluminum salophencompound.

Biphasic Carbonylation Catalysts

In some embodiments, the carbonylation catalyst is biphasic. Thus, incertain variations, the carbonylation reaction product mixture comprisesat least two phases, wherein one phase is a catalyst phase and a secondphase is a product phase, wherein following the carbonylation reaction,the majority of the carbonylation catalyst is located in the catalystphase, and the majority of the bPL produced is located in the productphase. For example, in some embodiments, between 50 wt % and 100 wt %,between 60 wt % and 100 wt %, between 70 wt % and 100 wt %, between 80wt % and 100 wt %, between 90 wt % and 100 wt %, or between 95 wt % and100 wt % of the carbonylation catalyst is located in the catalyst phase.In some embodiments, between 50 wt % and 100 wt %, between 60 wt % and100 wt %, between 70 wt % and 100 wt %, between 80 wt % and 100 wt %,between 90 wt % and 100 wt %, or between 95 wt % and 100 wt % of the bPLproduced is located in the product phase. In some embodiments, thebiphasic carbonylation catalyst is any of the carbonylation catalystsdescribed herein, provided the catalyst is at least partially immisciblewith bPL. In other embodiments, the carbonylation catalyst is any of thecarbonylation catalysts described herein modified to contain asubstituent to make the modified catalyst at least partially immisciblewith bPL.

In some embodiments, the carbonylation catalyst is at least partiallyimmiscible with bPL under certain conditions, but miscible with bPLunder other conditions. For example, in some variations, the biphasiccatalyst is completely miscible with bPL in the carbonylation productstream at one temperature and at least partially immiscible with bPL inthe carbonylation product stream at a lower temperature. In othervariations, the biphasic catalyst comprises one or more ionizablefunctional groups which enable the catalyst to be miscible with bPL inthe carbonylation product stream at one pH, and at least partiallyimmiscible at a different pH. Thus, in some embodiments, the biphasiccatalyst is combined with EO and CO at a first pH to produce bPL,wherein the biphasic catalyst is miscible with bPL, and then the pH ofthe reaction mixture is changed such that the biphasic catalyst is atleast partially immiscible with bPL.

Monitoring and Replacing Catalyst

In one aspect, the production system/production process is configuredfor continuous carbonylation of an epoxide or lactone feedstock, theprocess comprising the steps of: reacting an epoxide or lactonefeedstock with carbon monoxide in the presence of a catalyst comprisinga Lewis acid and a metal carbonyl in a carbonylation reaction vessel;measuring one or more parameters selected from the group consisting of:(i) a concentration of the Lewis acid, or a decomposition productthereof, within the carbonylation reaction vessel; (ii) a concentrationof the Lewis acid, or a decomposition product thereof, in a productstream downstream from the carbonylation reaction vessel; (iii) aconcentration of the metal carbonyl, or a decomposition product thereof,within the carbonylation reaction vessel; (iv) a concentration of themetal carbonyl, or a decomposition product thereof, in a product streamdownstream from the carbonylation reaction vessel; and (v) a rate of thecarbonylation reaction; comparing the measured value of the one or moreparameters to predetermined reference values for the one or moreparameters; and where the measured value of any one of parameters i),iii), or v) is less than the reference value, or where the measuredvalue of any one of parameters ii) or iv) is greater than the referencevalue, introducing to the carbonylation reaction vessel a catalystreplacement component which is different from the catalyst and comprisesa species selected from the group consisting of the Lewis acid, aprecursor to the Lewis acid, the metal carbonyl, and a precursor to themetal carbonyl.

In some embodiments, one of the one or more parameters measured is theconcentration of the Lewis acid, or a decomposition product thereof,within the carbonylation reaction vessel. In some embodiments, theconcentration of the Lewis acid within the carbonylation reaction vesselis measured. In some embodiments, the concentration of a decompositionproduct of the Lewis acid within the carbonylation reaction vessel ismeasured.

In some embodiments, one of the one or more parameters measured is theconcentration of the metal carbonyl, or a decomposition product thereof,within the carbonylation reaction vessel. In some embodiments, theconcentration of the metal carbonyl within the carbonylation reactionvessel is measured. In some embodiments, the concentration of adecomposition product of the metal carbonyl within the carbonylationreaction vessel is measured.

In some embodiments, one of the one or more parameters measured is theconcentration of the Lewis acid, or a decomposition product thereof, inthe product stream downstream from the carbonylation reaction vessel. Insome embodiments, the concentration of the Lewis acid in the productstream downstream from the carbonylation reaction vessel is measured. Insome embodiments, the concentration of a decomposition product of theLewis acid in the product stream downstream from the carbonylationreaction vessel is measured.

In some embodiments, one of the one or more parameters measured is theconcentration of the metal carbonyl, or a decomposition product thereof,in the product stream downstream from the carbonylation reaction vessel.In some embodiments, the concentration of the metal carbonyl in theproduct stream downstream from the carbonylation reaction vessel ismeasured. In some embodiments, the concentration of a decompositionproduct of the metal carbonyl in the product stream downstream from thecarbonylation reaction vessel is measured.

In some embodiments, one of the one or more parameters measured is therate of the carbonylation reaction. In some embodiments, the rate of thecarbonylation reaction is measured by the change in concentration of acarbonylation product in the carbonylation reaction vessel over time. Insome embodiments, the rate of the carbonylation reaction is measured bythe change in concentration of a carbonylation product in the productstream downstream from the carbonylation reaction vessel over time. Insome embodiments, the carbonylation product is a beta-propiolactone. Insome embodiments, the carbonylation product is beta-propiolactone (bPL).In some embodiments, the carbonylation product is a succinic anhydride.In some embodiments the carbonylation product is succinic anhydride(SA).

In some embodiments, the product stream is separated from thecarbonylation reaction vessel by a nanofiltration membrane. In someembodiments, the nanofiltration membrane is selected based on itsability to retain solutes having a molecular weight greater than themolecular weight of the epoxide or lactone carbonylation products, butless than the molecular weights of either the Lewis acid or the metalcarbonyl. In some embodiments, the nanofiltration membrane is designedto retain solutes having a molecular weight greater than the molecularweight of the epoxide or lactone carbonylation products, but less thanthe molecular weights of either the Lewis acid or the metal carbonyl.

In some embodiments, the catalyst replacement component comprises theLewis acid, or a precursor to the Lewis acid. In some embodiments, thecatalyst replacement component comprises the Lewis acid. In someembodiments, the catalyst replacement component comprises a precursor tothe Lewis acid.

In some embodiments, the catalyst replacement component comprises themetal carbonyl, or a precursor to the metal carbonyl. In someembodiments, the catalyst replacement component comprises the metalcarbonyl. In some embodiments, the catalyst replacement componentcomprises a precursor to the metal carbonyl.

In some embodiments, where more than one catalyst replacement componentis added, each of the one or more catalyst replacement components isadded to the carbonylation reaction vessel separately. In someembodiments, where more than one catalyst replacement component isadded, all of the one or more catalyst replacement components are addedto the carbonylation reaction vessel together.

In some embodiments, each of the one or more catalyst replacementcomponents is added individually to the carbonylation reaction vesselwithout solvent, as a solution in an organic solvent, or as a slurry. Insome embodiments, each of the one or more catalyst replacementcomponents is added to the carbonylation reaction vessel withoutsolvent. In some embodiments, each of the one or more catalystreplacement components is added to the carbonylation reaction vessel asa solution in an organic solvent. In some embodiments, each of the oneor more catalyst replacement components is added to the carbonylationreaction vessel as a slurry.

In certain embodiments, where more than one catalyst replacementcomponent are added, each catalyst replacement component is dissolved insolution, and the solutions are combined enroute to the vessel, e.g., byusing a mixing tee or flowing the combined solutions through a staticmixer.

In certain embodiments, fresh catalyst may also be added to the reactionvessel at the same or different times as the one or more catalystreplacement components.

In certain embodiments, the catalyst replacement components are addedunder an atmosphere comprising CO. In certain embodiments, the CO ispresent at a pressure from about 1 atmosphere to about 400 atmospheres.In certain embodiments, the catalyst replacement components are addedunder an atmosphere comprising CO at a pressure between about 1atmosphere and about 100 atmospheres, or between about 1 atmosphere andabout 50 atmospheres, or between about 10 atmospheres and about 20atmospheres, or between about 5 atmospheres and about 10 atmospheres, orbetween about 1 atmosphere and about 5 atmospheres.

In some embodiments, the amount of a given catalyst replacementcomponent added to the carbonylation reaction vessel is proportional toone of the parameters being measured in step (a). In some embodiments,the amount of a given catalyst replacement component is directlyproportional to changes in the concentration of the parameter measuredin the product stream downstream from the carbonylation reaction vessel.

In some embodiments, if the concentration of the Lewis acid, or adecomposition product thereof, measured in step (a) is increased in theproduct stream downstream from the carbonylation reaction vessel, anamount of Lewis acid that is proportional to the increase in theconcentration of Lewis acid, or a decomposition product thereof,measured in step (a) is added to the carbonylation reaction vessel. Insome embodiments, if the concentration of the Lewis acid, or adecomposition product thereof, measured in step (a) is decreased withinthe carbonylation reaction vessel, an amount of Lewis acid, or aprecursor to the Lewis acid, that is proportional to the decrease in theconcentration of Lewis acid, or a decomposition product thereof,measured in step (a) is added to the carbonylation reaction vessel. Forexample, if the concentration of the Lewis acid has decreased by 5%, anamount of the Lewis acid or precursor to the Lewis acid that isequivalent to about 5% of the amount of the Lewis acid initially chargedinto the carbonylation reaction vessel is added.

In some embodiments, if the rate of the carbonylation reaction, measuredin step (a) is decreased, an amount of Lewis acid, or a precursor to theLewis acid, that is proportional to the decrease in the rate of thecarbonylation reaction is added to the carbonylation reaction vessel. Insome embodiments, if the rate of the carbonylation reaction measured instep (a) is decreased, an amount of the metal carbonyl or a precursor tothe metal carbonyl that is proportional to the decrease in the rate ofthe carbonylation reaction is added to the carbonylation reactionvessel. For example, if the rate of the carbonylation reaction hasdecreased by 5%, an amount of Lewis acid, precursor to the Lewis acid,metal carbonyl, or precursor to the metal carbonyl that is equivalent toabout 5% of the amount of the Lewis acid or metal carbonyl initiallycharged into the carbonylation reaction vessel is added.

In some embodiments, if the concentration of the metal carbonyl,measured in step (a) is increased in the product stream downstream fromthe carbonylation reaction vessel, an amount of metal carbonyl, or aprecursor to the metal carbonyl that is proportional to the increase inthe amount of metal carbonyl measured in step (a) is added to thecarbonylation reaction vessel. In some embodiments, if the concentrationof the metal carbonyl, or a decomposition product thereof, measured instep (a) is decreased within the carbonylation reaction vessel, anamount of metal carbonyl, or a precursor to the metal carbonyl, that isproportional to the decrease in the amount of metal carbonyl, or adecomposition product thereof, measured in step (a) is added to thecarbonylation reaction vessel. For example, if the concentration of themetal carbonyl has decreased by 5%, an amount of the metal carbonyl orprecursor to the metal carbonyl that is equivalent to about 5% of theamount of the metal carbonyl initially charged into the carbonylationreaction vessel is added.

FIG. 14 includes carbonylation catalyst source 1403 that can feed freshcarbonylation catalyst in carbonylation catalyst stream 1407 tocarbonylation reaction system inlet 1409. Carbonylation catalyst canarrive to the carbonylation catalyst source as either solids (perhapsblanketed under CO or a suitable inert gas) or in solution of solventsuch as hexane or THF. If solid catalysts, the solids can be unpackedand loaded into one or more hoppers under inert conditions (for example,CO or inert gas). The solids from the one or more hoppers can be meteredinto a suitable solvent before pumping. In some embodiments, the solidcatalyst (or liquid catalyst) or catalyst precursors can be dispensedfrom a shipping vessel/container into an intermediate inert vessel to bemixed with solvent and then pumped. In some embodiments, the catalystpreparation system and connections are selected such that thecatalyst/precursors are not exposed to the atmosphere. Carbonylationcatalyst solutions can be suitable for direct pumping to thecarbonylation reaction system. In some embodiments, the carbonylationcatalyst feed is pumped under CO pressure to help ensure stability ofthe catalyst. Furthermore, carbonylation catalyst source and feed can becooled below ambient temperature to ensure stability. In someembodiments, the inlet to the carbonylation reaction system can receivecarbonylation catalyst from a carbonylation catalyst source at betweenabout 0.01 to 50 kg/hr, between about 0.01 to 40 kg/hr, between about0.01 to 30 kg/hr, between about 0.01 to 20 kg/hr, between about 0.01 to10 kg/hr, between about 0.2-5 kg/hr, between about 0.5-4 kg/hr, betweenabout 1-3 kg/hr, between about 1-2 kg/hr, or about 1.4 kg/hr. In someembodiments, the inlet to the carbonylation reaction system can receivecarbonylation catalyst from a carbonylation catalyst source at betweenabout 0.0001-10 kmol/hr, between about 0.0001-1 kmol/hr, between about0.0001-0.1 kmol/hr, between about 0.0001-0.01 kmol/hr, between about0.0005-0.001 kmol/hr, between about 0.0005-0.005 kmol/hr, or about 0.001kmol/hr, or about 0.01 kmol/hr, or about 0.1 kmol/hr. In someembodiments, the carbonylation catalyst can be in a solvent such as THFso that the mass fraction of carbonylation catalyst in the stream fromthe carbonylation catalyst source can be between about 0.001-0.1, about0.005-0.05, about 0.01-0.05, or about 0.02. In some embodiments, theinlet to the carbonylation reaction system can receive carbonylationcatalyst from a carbonylation catalyst source at a temperature betweenabout 10-30° C., between about 15-25° C., or about 20° C. In someembodiments, the inlet to the carbonylation reaction system can receivecarbonylation catalyst from a carbonylation catalyst source at apressure of at least about 50 bar, about 60-70 bar, or at least about 65bar.

Carbon Monoxide Source

Carbon monoxide is fed into the β-propiolactone productionsystem/production process at an amount sufficient to carbonylateethylene oxide to produce β-propiolactone. In some variations, this maybe achieved performing the carbonylation reaction under asuperatmospheric pressure of carbon monoxide. In certain embodiments,the carbon monoxide is provided into the β-propiolactone productionsystem/production process at a pressure in the range from about 50 psi(350 kPa) to about 5000 psi (35 MPa). In certain embodiments, the carbonmonoxide is provided into the β-propiolactone productionsystem/production process at a pressure from about 50 psi (350 kPa) toabout 1000 psi (7 MPa). In certain embodiments, the carbon monoxide isprovided into the β-propiolactone production system/production processat a pressure from about 50 psi (350 kPa) to about 500 psi (3.5 MPa). Incertain embodiments, the carbon monoxide is provided into theβ-propiolactone production system/production process at a pressure fromabout 100 psi (700 kPa) to about 400 psi (2.8 MPa). In certainembodiments, the carbon monoxide is provided into the β-propiolactoneproduction system/production process at a pressure of about 200 psi (1.4MPa). In certain embodiments, the carbon monoxide is provided into theβ-propiolactone production system/production process under an atmospherehaving a partial pressure of CO of about 200 psi (1.4 MPa). Thesuperatmospheric pressure of carbon monoxide may be provided in the formof pure carbon monoxide, or by providing a gas mixture containing carbonmonoxide. In certain embodiments, the carbon monoxide may be provided inthe form of substantially pure carbon monoxide. In other embodiments,the carbon monoxide may be provided in the form of carbon monoxide mixedwith one or more inert gases. In other embodiments, the carbon monoxidemay be provided in the form of a mixture of carbon monoxide andhydrogen. In certain embodiments, the carbon monoxide may be provided inthe form of a carbon monoxide-containing industrial process gas such assyngas, coal gas, wood gas, or the like.

FIG. 14 includes carbon monoxide source 1411 that can feed carbonmonoxide to carbonylation reaction system inlet 1409. In someembodiments, the carbon monoxide source that supplies carbon monoxide tothe carbonylation reaction system can include fresh carbon monoxidesource 1401 (i.e., main CO feed) and recycled carbon monoxide stream1410 from the carbonylation reaction system. In some embodiments, thecarbon monoxide source can be only the fresh carbon monoxide source. Insome embodiments, the carbon monoxide source can be only the recycledcarbon monoxide. In some embodiments, fresh carbon monoxide stream 1405and/or the recycled carbon monoxide streams can be fed into carbonmonoxide compressor 1401A prior to the resultant stream from the carbonmonoxide compressor (i.e., reactor carbon monoxide inlet stream) beingfed into the carbonylation reaction system. In some embodiments,resultant stream from the carbon monoxide compressor 1411 (i.e.,reaction system carbon monoxide inlet stream) can be the carbon monoxidesource. The carbon monoxide source can be compressed to the pressure ator above the carbonylation reaction system pressure and then fed to thecarbonylation system. In some embodiments, the fresh carbon monoxidesource (i.e., main CO feed) and the recycled carbon monoxide can becompressed in separate compressors. One reason recycled carbon monoxidecan be compressed separately from the fresh carbon monoxide feed (i.e.,main CO feed) to reaction system pressure is to avoid contamination ofthe main compressor (i.e., fresh feed compressor) with hazardouscomponents such as ethylene oxide and bPL that may be present in thecarbon monoxide recycle stream. Some of these potentially hazardouscomponents may be removed from the compressor as partially liquefiedcomponents as waste. In some embodiments, these potentially hazardouscomponents can also be recycled to the carbonylation reaction system. Insome embodiments, the compressed carbon monoxide from both compressorscan be fed to the carbonylation reaction system as the reaction systemcarbon monoxide inlet stream.

In some embodiments, the fresh carbon monoxide source can provide atleast about 1000 kg/hr CO, at least about 1200 kg/hr CO, at least about1400 kg/hr CO, at least about 1500 kg/hr CO, at least about 1600 kg/hrCO, at least about 2000 kg/hr CO, at least about 4000 kg/hr CO, at leastabout 5000 kg/hr CO, at least about 10000 kg/hr CO, at least about 12000kg/hr CO, at least about 14000 kg/hr CO, at least about 15000 kg/hr CO,or at least about 16000 kg/hr CO. In some embodiments, the fresh carbonmonoxide source can provide at least about 30 kmol/hr CO, at least about40 kmol/hr CO, at least about 50 kmol/hr CO, at least about 55 kmol/hrCO, or at least about 60 kg/hr CO. In some embodiments, the fresh carbonmonoxide source can provide about 1000 kg/hr CO to about 16000 kg/hr CO,about 1200 kg/hr CO to about 16000 kg/hr CO, about 1400 kg/hr CO toabout 16000 kg/hr CO, about 1500 kg/hr CO to about 16000 kg/hr CO, about1600 kg/hr CO to about 16000 kg/hr CO, about 2000 kg/hr CO to about16000 kg/hr CO, about 4000 kg/hr CO to about 16000 kg/hr CO, about 6000kg/hr CO to about 16000 kg/hr CO, about 1000 kg/hr CO to about 16000kg/hr CO, or about 1400 kg/hr CO to about 16000 kg/hr CO. In someembodiments, the fresh carbon monoxide source can provide about 1000kg/hr CO, about 1200 kg/hr CO, about 1400 kg/hr CO, about 1500 kg/hr CO,about 1600 kg/hr CO, about 1800 kg/hr CO, about 2000 kg/hr CO, about2400 kg/hr CO, about 2600 kg/hr CO, about 2800 kg/hr CO, about 3000kg/hr CO, about 3200 kg/hr CO, about 4000 kg/hr CO, about 6000 kg/hr CO,about 8000 kg/hr CO, about 10000 kg/hr CO, about 12000 kg/hr CO, about14000 kg/hr CO, or about 16000 kg/hr CO. In some embodiments, the freshcarbon monoxide source can provide at least about 30 kmol/hr CO, atleast about 40 kmol/hr CO, at least about 50 kmol/hr CO, at least about55 kmol/hr CO, at least about 60 kmol/hr CO, at least about 100 kmol/hrCO, at least about 150 kmol/hr CO, at least about 200 kmol/hr CO, atleast about 250 kmol/hr CO, at least about 300 kg/hr CO, at least about350 kmol/hr CO, at least about 400 kmol/hr CO, at least about 500kmol/hr CO, at least about 550 kmol/hr CO, or at least about 600 kg/hrCO. In some embodiments, the fresh carbon monoxide source can provideabout 30 kmol/hr CO to about 60 kmol/hr CO, about 40 kmol/hr CO to about60 kmol/hr CO, about 50 kmol/hr CO to about 60 kmol/hr CO, about 30kmol/hr CO to about 600 kmol/hr CO, about 40 kmol/hr CO to about 600kmol/hr CO, about 50 kmol/hr CO to about 600 kmol/hr CO, about 55kmol/hr CO to about 600 kmol/hr CO, about 100 kmol/hr CO to about 600kmol/hr CO, about 200 kg/hr CO to about 600 kmol/hr CO, about 300kmol/hr CO to about 600 kmol/hr CO, about 400 kmol/hr CO to about 600kmol/hr CO, about 500 kmol/hr CO to about 600 kmol/hr CO, about 525kmol/hr CO to about 600 kmol/hr CO, about 550 kg/hr CO to about 600kmol/hr CO. In some embodiments, the fresh carbon monoxide from thefresh carbon monoxide source may have some impurities and thus mayrequire additional purification steps such as adsorption. In someembodiments, the flow rate from the fresh carbon monoxide source is setto about the stoichiometric value for the carbonylation reaction, toabout 5% higher than the stoichiometric value, to about 10% higher thanthe stoichiometric value, to about 15% higher than the stoichiometricvalue, or to about 20% higher than the stoichiometric value.

In some embodiments, the recycled carbon monoxide from the carbonylationreaction system can provide at least about 100 kg/hr CO, at least about150 kg/hr CO, at least about 200 kg/hr CO, at least about 255 kg/hr CO,at least about 300 kg/hr CO, at least about 350 kg/hr CO, at least about500 kg/hr CO, at least about 600 kg/hr CO, at least about 800 kg/hr CO,at least about 1000 kg/hr CO, at least about 1250 kg/hr CO, at leastabout 1500 kg/hr CO, at least about 1750 kg/hr CO, at least about 2000kg/hr CO, at least about 2500 kg/hr CO, at least about 3000 kg/hr CO, orat least about 3500 kg/hr CO. In some embodiments, the recycled carbonmonoxide from the carbonylation reaction system can provide from about100 kg/hr CO to about 350 kg/hr CO, about 150 kg/hr CO to about 350kg/hr CO, about 200 kg/hr CO to about 350 kg/hr CO, about 255 kg/hr COto about 350 kg/hr CO, about 300 kg/hr CO to about 350 kg/hr CO, fromabout 100 kg/hr CO to about 3500 kg/hr CO, about 150 kg/hr CO to about3500 kg/hr CO, about 200 kg/hr CO to about 3500 kg/hr CO, about 255kg/hr CO to about 3500 kg/hr CO, about 300 kg/hr CO to about 3500 kg/hrCO, about 350 kg/hr CO to about 3500 kg/hr CO, about 1000 kg/hr CO toabout 3500 kg/hr CO, about 1500 kg/hr CO to about 3500 kg/hr CO, about2000 kg/hr CO to about 3500 kg/hr CO, about 2550 kg/hr CO to about 3500kg/hr CO, about 3000 kg/hr CO to about 3500 kg/hr CO. In someembodiments, the recycled carbon monoxide from the carbonylationreaction system can provide about 100 kg/hr CO, about 150 kg/hr CO,about 200 kg/hr CO, about 255 kg/hr CO, about 300 kg/hr CO, about 350kg/hr CO, about 500 kg/hr CO, about 750 kg/hr CO, about 1000 kg/hr CO,about 1250 kg/hr CO, about 1500 kg/hr CO, about 2000 kg/hr CO, about2500 kg/hr CO, about 3000 kg/hr CO, or about 3500 kg/hr CO. In someembodiments, the recycled carbon monoxide source can provide at leastabout 3 kmol/hr CO, at least about 5 kmol/hr CO, at least about 7kmol/hr CO, at least about 9 kmol/hr CO, at least about 10 kmol/hr CO,at least about 15 kmol/hr CO, at least 50 kmol/hr CO, at least 100kmol/hr CO, or at least 150 kmol/hr CO. In some embodiments, the massfraction of CO in the recycled carbon monoxide stream can be at leastabout 0.70, at least about 0.75, at least about 0.8, or at least about0.85. In some embodiments, the mole fraction of CO in the recycledcarbon monoxide stream can be at least about 0.70, at least about 0.75,at least about 0.8, at least about 0.85, at least about 0.896, at leastabout 0.9, or at least about 0.95. In some embodiments, the molefraction of CO in the recycled carbon monoxide stream can be 0.70 to1.0, 0.75 to 1.0, 0.8 to 1.0, 0.85 to 1.0, 0.896 to 1.0, 0.9 to 1.0, or0.95 to 1.0. The recycled carbon monoxide stream from the carbonylationreaction system can also include unreacted ethylene oxide (in about atmost 10 kg/hr, at most 15 kg/hr, at most 20 kg/hr, at most 25 kg/hr, atmost 50 kg/hr, at most 75 kg/hr, at most 100 kg/hr, at most 150 kg/hr,at most 200 kg/hr, or at most 250 kg/hr or a mass fraction of betweenabout 0.05-0.075, about 0.055-0.07, about 0.06-0.07, about at most0.065, about at most 0.07, or about at most 0.075), secondary reactionproduct acetaldehyde (in about at most 0.5 kg/hr, at most about 1 kg/hr,at most about 1.3 kg/hr, at most about 2 kg/hr, at most about 4 kg/hr,at most about 6 kg/hr, at most about 10 kg/hr, at most about 13 kg/hr ora mass fraction of about 0.001-0.009, about 0.003-0.005, or about most0.004, about at most 0.005, or at most about 0.009), bPL (in about atmost about 0.005 kg/hr, at most about 0.01 kg/hr, at most about 0.015kg/hr, about at most about 0.019 kg/hr, at most about 0.05 kg/hr, atmost about 0.1 kg/hr, at most about 0.15 kg/hr, or about at most about0.19 kg/hr), and the remainder solvent (e.g., THF).

In some embodiments, the inlet to the carbonylation reaction system canreceive carbon monoxide from a carbon monoxide source at least about1000 kg/hr, at least about 1250 kg/hr, at least about 1500 kg/hr, atleast about 1600 kg/hr, at least about 1655 kg/hr, at least about 1700kg/hr, at least about 4000 kg/hr, at least about 5000 kg/hr, at leastabout 700 kg/hr, at least about 8500 kg/hr, at least about 10000 kg/hr,at least about 12500 kg/hr, at least about 15000 kg/hr, at least about16000 kg/hr, at least about 16550 kg/hr, or at least about 17000 kg/hr.In some embodiments, the inlet to the carbonylation reaction system canreceive carbon monoxide from a carbon monoxide source at about 1000kg/hr to about 1700 kg/hr, about 1250 kg/hr to about 1700 kg/hr, about1500 kg/hr to about 1700 kg/hr, about 1600 kg/hr to about 1700 kg/hr,about 1655 kg/hr to about 1700 kg/hr, 1000 kg/hr to about 17000 kg/hr,about 1250 kg/hr to about 17000 kg/hr, about 1500 kg/hr to about 17000kg/hr, about 1600 kg/hr to about 17000 kg/hr, about 1655 kg/hr to about17000 kg/hr, about 1700 kg/hr to about 17000 kg/hr, at about 2000 kg/hrto about 17000 kg/hr, about 3000 kg/hr to about 17000 kg/hr, about 4000kg/hr to about 17000 kg/hr, about 6000 kg/hr to about 17000 kg/hr, about8000 kg/hr to about 17000 kg/hr, about 1200 kg/hr to about 17000 kg/hr,about 1400 kg/hr to about 17000 kg/hr, about 1500 kg/hr to about 17000kg/hr, or about 1600 kg/hr to about 17000 kg/hr. In some embodiments,the inlet to the carbonylation reaction system can receive carbonmonoxide from a carbon monoxide source at about 1000 kg/hr, about 1250kg/hr, about 1500 kg/hr, about 1600 kg/hr, about 1655 kg/hr, about 1700kg/hr, about 2000 kg/hr, about 1900 kg/hr, about 2500 kg/hr, about 3000kg/hr, about 4000 kg/hr, about 6000 kg/hr, about 8000 kg/hr, about 10000kg/hr, about 12000 kg/hr, about 13000 kg/hr, about 14000 kg/hr, about15000 kg/hr, about 16000 kg/hr, or about 17000 kg/hr. In someembodiments, the inlet to the carbonylation reaction system can receivecarbon monoxide from a carbon monoxide source at least about 35 kmol/hr,at least about 45 kmol/hr, at least about 50 kmol/hr, at least about 55kmol/hr, or at least about 59 kmol/hr. As previously discussed, in someembodiments, the carbon monoxide source can include some recycled carbonmonoxide from the carbonylation reaction system. Accordingly, in someembodiments, the inlet to the carbonylation reaction system can alsoreceive ethylene oxide (in about 5-300 kg/hr, about 10-200 kg/hr, about10-100 kg/hr, about 10-50 kg/hr, about 10-30 kg/hr, about 10-20 kg/hr,or at most about 15 kg/hr, at most about 50 kg/hr, at most about 100kg/hr, at most about 150 kg/hr, at most about 200 kg/hr, at most about300 kg/hr, or a mass fraction of about 0.001-0.05, about 0.005-0.02, orat most about 0.009, at most about 0.02, or at most about 0.05),acetaldehyde (in about 0.25-15 kg/hr, about 0.5-12.5 kg/hr, about0.25-10 kg/hr, about 0.5-5 kg/hr, about 0.25-1.5 kg/hr, about 0.5-1.25kg/hr, or at most about 0.9 kg/hr, at most about 1.5 kg/hr, at mostabout 3 kg/hr, at most about 6 kg/hr, at most about 12 kg/hr, at mostabout 15 kg/hr, or a mass fraction of about 0.001-0.05, about0.005-0.02, or at most about 0.009, at most about 0.02, or at most about0.05), and the remainder solvent from the carbon monoxide source. Insome embodiments, the mass fraction of CO from the carbon monoxidesource can be at least about 0.9, at least about 0.95, at least about0.985, or at least about 0.99. In some embodiments, the mole fraction ofCO from the carbon monoxide source can be at least about 0.9, at leastabout 0.95, at least about 0.98, at least about 0.99, or at least about0.995. In some embodiments, the mole fraction of CO from the carbonmonoxide source can be 0.9 to 1.0, 0.95 to 1.0, 0.98 to 1.0, 0.99 to1.0, or 0.995 to 1.0.

In some embodiments, the inlet to the carbonylation reaction system canreceive carbon monoxide from a carbon monoxide source at a temperaturebetween about 10-170° C., between about 30-70° C., between about 40-60°C., between about 45-55° C., or about 50° C. In some embodiments, theinlet to the carbonylation reaction system can receive carbon monoxidefrom a carbon monoxide source at a pressure of at least about 50 bar,about 60-70 bar, or at least about 65 bar.

Solvent Source

The solvent may be selected from any solvents described herein, andmixtures of such solvents. In some variations, the solvent is an organicsolvent. In certain variations, the solvent is an aprotic solvent.

In some embodiments, the solvent includes dimethylformamide, N-methylpyrrolidone, tetrahydrofuran, toluene, xylene, diethyl ether,methyl-tert-butyl ether, acetone, methylethyl ketone, methyl-iso-butylketone, butyl acetate, ethyl acetate, dichloromethane, and hexane, andmixtures of any two or more of these. In general polar aprotic solventsor hydrocarbons are suitable for this step.

Additionally, in one variation, β-lactone may be utilized as aco-solvent. In other variations, the solvent may include ethers,hydrocarbons and non protic polar solvents. In some embodiments, thesolvent includes tetrahydrofuran (“THF”), sulfolane, N-methylpyrrolidone, 1,3 dimethyl-2-imidazolidinone, diglyme, triglyme,tetraglyme, diethylene glycol dibutyl ether, isosorbide ethers, methyltertbutyl ether, diethylether, diphenyl ether, 1,4-dioxane, ethylenecarbonate, propylene carbonate, butylene carbonate, dibasic esters,diethyl ether, acetonitrile, ethyl acetate, dimethoxy ethane, acetone,and methylethyl ketone. In other embodiments, the solvent includestetrahydrofuran, tetrahydropyran, 2,5-dimethyl tetrahydrofuran,sulfolane, N-methyl pyrrolidone, 1,3 dimethyl-2-imidazolidinone,diglyme, triglyme, tetraglyme, diethylene glycol dibutyl ether,isosorbide ethers, methyl tertbutyl ether, diethylether, diphenyl ether,1,4-dioxane, ethylene carbonate, propylene carbonate, butylenecarbonate, dibasic esters, diethyl ether, acetonitrile, ethyl acetate,propyl acetate, butyl acetate, 2-butanone, cyclohexanone, toluene,difluorobenzene, dimethoxy ethane, acetone, and methylethyl ketone. Incertain variations, the solvent is a polar donating solvent. In onevariation, the solvent is THF.

In some embodiments, the catalyst and/or solvent stream is recycled tothe feed stream or to the carbonylation reaction system. In someembodiments, the portion of the solvent and/or catalyst from thereaction product stream recycled to the carbonylation reactor or feedstream ranges from about 0% to about 100%. In some embodiments, theportion of the solvent and/or catalyst from the reaction product streamrecycled to the carbonylation reactor or feed stream is about 100%,about 90%, about 80%, about 70%, about 60%, about 50%, about 40%, about30%, about 20%, about 10%, or about 0%. In some embodiments, a differentpercentage of the catalyst, as compared to the solvent is recycled,i.e., the proportions of either the catalyst or solvent component do notneed to be equal.

Referring again to the exemplary system depicted in FIG. 14, in someembodiments, solvent feed 1424 can supply solvent to the carbonylationreaction system inlet 1409. Solvent can be fed to the carbonylationreaction system suing a pump. In addition, the solvent streams, sources,storage tanks, etc, can be maintained under an inert or CO atmosphere.In some embodiments, the solvent feed that supplies solvent to thecarbonylation reaction system can include solvent 1408 from freshsolvent source 1404, recycled solvent 1423 from the BPL purificationsystem, and/or solvent in recycled carbonylation catalyst stream 1412from the carbonylation catalyst isolation system. In some embodiments,the recycled solvent from the BPL purification system can be stored in amake-up solvent reservoir. In some embodiments, the solvent feed thatsupplies solvent to the carbonylation reaction system can includesolvent from the make-up solvent reservoir. In some embodiments, solventcan be purged from the system. In some embodiments, the purged solventcan be solvent from the recycled solvent of the BPL purification system.In some embodiments, solvent from the fresh solvent source is alsostored into the make-up solvent reservoir to dilute the recycled solventfrom the BPL purification system with fresh solvent. In someembodiments, fresh solvent is fed from the fresh solvent source to themake-up solvent reservoir prior to entering the carbonylation reactionsystem. In some embodiments, solvent from the fresh solvent source, theBPL purification system, and the carbonylation catalyst isolation systemcan be purified by operations such as adsorption to remove oxygen andwater that can inhibit the carbonylation catalyst. In some embodiments,the amount of oxygen and/or water in all streams entering thecarbonylation reaction system is less than about 500 ppm, less thanabout 250 ppm, less than about 100 ppm, less than about 50 ppm, lessthan about 20 ppm, less than about 10 ppm, less than about 5 ppm, lessthan about 2 ppm, or less than about 1 ppm.

In some embodiments, the fresh solvent source can provide at least about50 kg/hr solvent, at least about 100 kg/hr solvent, at least about 150kg/hr solvent, at least about 188 kg/hr solvent, at least about 200kg/hr solvent, at least about 250 kg/hr solvent, at least about 500kg/hr solvent, at least about 1000 kg/hr solvent, at least about 1500kg/hr solvent, at least about 1880 kg/hr solvent, at least about 2000kg/hr solvent, or at least about 2500 kg/hr solvent. In someembodiments, the fresh solvent source can provide about 50 kg/hr toabout 250 kg/hr solvent, about 100 kg/hr to about 250 kg/hr solvent,about 150 kg/hr to about 250 kg/hr solvent, about 188 kg/hr to about 250kg/hr solvent, about 200 kg/hr to about 250 kg/hr solvent, about 50kg/hr to about 2500 kg/hr solvent, about 100 kg/hr to about 2500 kg/hrsolvent, about 150 kg/hr to about 2500 kg/hr solvent, about 188 kg/hr toabout 2500 kg/hr solvent, about 200 kg/hr to about 2500 kg/hr solvent,about 250 kg/hr to about 2500 kg/hr solvent, about 500 kg/hr to about2500 kg/hr solvent, about 1000 kg/hr to about 2500 kg/hr solvent, about1500 kg/hr to about 2500 kg/hr solvent, about 1880 kg/hr to about 2500kg/hr solvent, about 2000 kg/hr to about 2500 kg/hr solvent, or about2250 kg/hr to about 2500 kg/hr solvent. In some embodiments, the freshsolvent source can provide about 50 kg/hr solvent, about 100 kg/hrsolvent, about 150 kg/hr solvent, about 188 kg/hr solvent, about 200kg/hr solvent, about 250 kg/hr solvent, about 500 kg/hr solvent, about1000 kg/hr solvent, about 1500 kg/hr solvent, about 1880 kg/hr solvent,about 2000 kg/hr solvent, or about 2500 kg/hr solvent. In someembodiments, the fresh solvent source can provide at least about 1kmol/hr solvent, at least about 2 kmol/hr solvent, at least about 2.6kmol/hr solvent, at least about 3 kmol/hr solvent, at least about 50kmol/hr solvent, at least about 100 kmol/hr solvent, at least about 150kmol/hr solvent, at least about 250 kmol/hr solvent, at least about 400kmol/hr solvent, or at least about 500 kmol/hr solvent.

In some embodiments, the recycled solvent from the BPL purificationsystem can provide at least about 8000 kg/hr solvent, at least about9000 kg/hr solvent, at least about 10000 kg/hr solvent, at least about10444 kg/hr solvent, at least about 12000 kg/hr solvent, at least about80000 kg/hr solvent, at least about 90000 kg/hr solvent, at least about100000 kg/hr solvent, at least about 104440 kg/hr solvent, or at leastabout 120000 kg/hr solvent. In some embodiments, the recycled solventfrom the BPL purification system can provide between about 8000 kg/hr toabout 12000 kg/hr solvent, between about 9000 kg/hr to about 12000 kg/hrsolvent, between about 10000 kg/hr to about 12000 kg/hr solvent, betweenabout 10444 kg/hr to about 12000 kg/hr solvent, about 8000 kg/hr toabout 120000 kg/hr solvent, between about 9000 kg/hr to about 120000kg/hr solvent, between about 10000 kg/hr to about 120000 kg/hr solvent,between about 10444 kg/hr to about 120000 kg/hr solvent, between about12000 kg/hr to about 120000 kg/hr solvent, about 40000 kg/hr to about120000 kg/hr solvent, about 60000 kg/hr to about 120000 kg/hr solvent,about 80000 kg/hr to about 120000 kg/hr solvent, between about 90000kg/hr to about 120000 kg/hr solvent, between about 100000 kg/hr to about120000 kg/hr solvent, between about 104440 kg/hr to about 120000 kg/hrsolvent, or between about 120000 kg/hr to about 120000 kg/hr solvent. Insome embodiments, the recycled solvent from the BPL purification systemcan provide about 8000 kg/hr solvent, about 9000 kg/hr solvent, about10000 kg/hr solvent, about 10444 kg/hr solvent, or about 12000 kg/hrsolvent. In some embodiments, the recycled solvent from the BPLpurification system can provide at least about 100 kmol/hr solvent, atleast about 120 kmol/hr solvent, at least about 140 kmol/hr solvent, atleast about 145 kmol/hr solvent, at least about 150 kmol/hr solvent, atleast 250 kmol/hr solvent, at least 350 kmol/hr solvent, or at least 500kmol/hr solvent. In some embodiments, the mass fraction of solvent inthe recycled solvent stream can be at least about 0.85, at least about0.90, at least about 0.95, or at least about 0.995. In some embodiments,the mole fraction of solvent in the recycled solvent stream can be atleast about 0.85, at least about 0.90, at least about 0.95, at leastabout 0.98, at least about 0.99, or at least about 0.993. In someembodiments, the mole fraction of solvent in the recycled solvent streamcan be 0.85 to 1.0, 0.90 to 1.0, 0.95 to 1.0, 0.98 to 1.0, 0.99 to 1.0,or 0.993 to 1.0. In some embodiments, the mole fraction of solvent inthe recycled solvent stream can be about 0.85, about 0.90, about 0.95,about 0.98, about 0.99, or about 0.993. The recycled solvent stream fromthe BPL purification system can also include unreacted carbon monoxide(in about at most 0.001 kg/hr, at most about 0.0025 kg/hr, at most about0.005 kg/hr, at most about 0.01 kg/hr, at most 0.02 kg/hr, at most about0.025 kg/hr, at most about 0.05 kg/hr, or at most about 0.01 kg/hr orbetween 0 and 0.005 kg/hr, or between 0 and 0.05 kg/hr) unreactedethylene oxide (in about at most about 10 kg/hr, at most about 20 kg/hr,at most about 30 kg/hr, at most about 33 kg/hr, at most about 50 kg/hr,at most about 100 kg/hr, at most about 200 kg/hr, or at most about 330kg/hr, or a mass fraction of between about 0.001-0.005, about0.02-0.004, or at most about 0.003, at most about 0.004, or at mostabout 0.005), secondary reaction product acetaldehyde (in about at most3 kg/hr, at most about 5 kg/hr, at most about 8.2 kg/hr, at most about10 kg/hr, at most about 15 kg/hr, at most 30 kg/hr, at most about 50kg/hr, or at most about 82 kg/hr or a mass fraction of at most about0.001, or between 0 and 8.2 kg/hr), and bPL (in at most about 2 kg/hr,at most about 3 kg/hr, at most about 5 kg/hr, at most about 7 kg/hr, atmost about 10 kg/hr, at most about 25 kg/hr, at most about 50 kg/hr, orat most about 70 kg/hr or a mass fraction of at most about 0.001, orbetween 0 and 7 kg/hr, or between 0 and 70 kg/hr).

In some embodiments, the recycled carbonylation catalyst stream from thecarbonylation catalyst isolation system can provide at least about 1000kg/hr solvent, at least about 1500 kg/hr solvent, at least about 1700kg/hr solvent, at least about 1840 kg/hr solvent, at least about 2000kg/hr solvent, at least about 5000 kg/hr solvent, at least about 10000kg/hr solvent, at least about 15000 kg/hr solvent, at least about 17000kg/hr solvent, at least about 18400 kg/hr solvent, or at least about20000 kg/hr solvent. In some embodiments, the recycled carbonylationcatalyst stream from the carbonylation catalyst isolation system canprovide about 1000 kg/hr to about 2000 kg/hr solvent, about 1500 kg/hrto about 2000 kg/hr solvent, about 1700 kg/hr to about 2000 kg/hrsolvent, about 1840 kg/hr to about 2000 kg/hr solvent, about 1000 kg/hrto about 20000 kg/hr solvent, about 1500 kg/hr to about 20000 kg/hrsolvent, about 1700 kg/hr to about 20000 kg/hr solvent, about 1840 kg/hrto about 20000 kg/hr solvent, about 2000 kg/hr to about 20000 kg/hrsolvent, about 5000 kg/hr to about 20000 kg/hr solvent, about 7500 kg/hrto about 20000 kg/hr solvent, about 12500 kg/hr to about 20000 kg/hrsolvent, about 15000 kg/hr to about 20000 kg/hr solvent, or about 17500kg/hr to about 20000 kg/hr solvent. In some embodiments, the recycledcarbonylation catalyst stream from the carbonylation catalyst isolationsystem can provide about 1000 kg/hr solvent, about 1500 kg/hr solvent,about 1700 kg/hr solvent, about 1840 kg/hr solvent, about 2000 kg/hrsolvent, about 2500 kg/hr solvent, about 3000 kg/hr solvent, about 5000kg/hr solvent, about 7000 kg/hr solvent, about 10000 kg/hr solvent,about 12500 kg/hr solvent, about 15000 kg/hr solvent, or about 20000kg/hr solvent. In some embodiments, the recycled carbonylation catalyststream from the carbonylation catalyst isolation system can provide atleast about 10 kmol/hr solvent, at least about 15 kmol/hr solvent, atleast about 20 kmol/hr solvent, at least about 25 kmol/hr solvent, atleast about 30 kmol/hr solvent, at least about 50 kmol/hr solvent, atleast about 75 kmol/hr solvent, at least about 100 kmol/hr solvent, atleast about 150 kmol/hr solvent, at least about 175 kmol/hr solvent, atleast about 200 kmol/hr solvent, at least about 250 kmol/hr solvent, orat least about 300 kmol/hr solvent In some embodiments, the massfraction of solvent in the recycled carbonylation catalyst stream can beat least about 0.60, at least about 0.65, at least about 070, or atleast about 0.74. In some embodiments, the mole fraction of solvent inthe recycled carbonylation catalyst stream can be at least about 0.60,at least about 0.65, at least about 0.70, at least about 0.75, at leastabout 0.80, or at least about 0.85. In some embodiments, the recycledcarbonylation catalyst stream from the carbonylation catalyst isolationsystem can also include unreacted carbon monoxide (in about at most 0.5kg/hr, at most about 1 kg/hr, at most about 1.2 kg/hr, at most about 1.5kg/hr, at most 5 kg/hr, at most about 10 kg/hr, at most about 12 kg/hr,or at most about 15 kg/hr, or a mass fraction of at most about 0.001),unreacted ethylene oxide (in about at most about 10 kg/hr, at most about20 kg/hr, at most 30 kg/hr, at most 33 kg/hr, at most about 100 kg/hr,at most about 200 kg/hr, at most 300 kg/hr, or at most 330 kg/hr or amass fraction of between about 0.005-0.01, about 0.01-0.05, or at mostabout 0.014, or at most about 0.10), secondary reaction productacetaldehyde (in about at most 1 kg/hr, at most about 2 kg/hr, at mostabout 3.3 kg/hr, at most 10 kg/hr, at most about 20 kg/hr, or at mostabout 33 kg/hr or a mass fraction of at most about 0.01), secondaryreaction product succinic anhydride (in about at most 1 kg/hr, at mostabout 2 kg/hr, at most about 3 kg/hr, at most 10 kg/hr, at most about 20kg/hr, or at most about 30 kg/hr or a mass fraction of at most about0.01), bPL (in about at most about 250 kg/hr, at most about 400 kg/hr,at most about 500 kg/hr, at most about 545 kg/hr, at most about 1000kg/hr, at most about 2500 kg/hr, at most about 4000 kg/hr, or at mostabout 5450 kg/hr or a mass fraction of at most about 0.1, at most about0.15, at most about 0.2, at most about 0.22, or at most about 0.23), andcarbonylation catalyst or components thereof.

Carbonylation catalyst components may include, for example, compoundsproduced by degradation of the catalyst, compounds used to produce thecatalyst, metals or metal ions which were part of the catalyst, anyorganic compounds which were part of the catalyst, metal carbonyls ormetal complexes which were part of the catalyst. For example, in someembodiments, carbonylation catalyst components are carbonyl cobaltate,aluminum salen compounds, aluminum porphyrin compounds, aluminumsalophen compounds, cobalt or cobalt ions, or aluminum or aluminum ions,or any combinations thereof.

In some embodiments, the recycled carbonylation catalyst stream from thecarbonylation catalyst isolation system can provide at least about 25kg/hr carbonylation catalyst, at least about 35 kg/hr carbonylationcatalyst, at least about 45 kg/hr carbonylation catalyst, at least about50 kg/hr carbonylation catalyst, at least about 53 kg/hr carbonylationcatalyst, at least about 100 kg/hr carbonylation catalyst, at leastabout 250 kg/hr carbonylation catalyst, at least about 350 kg/hrcarbonylation catalyst, at least about 450 kg/hr carbonylation catalyst,at least about 500 kg/hr carbonylation catalyst, at least about 530kg/hr carbonylation catalyst. In some embodiments, the recycledcarbonylation catalyst stream from the carbonylation catalyst isolationsystem can provide at least about 0.01 kmol/hr carbonylation catalyst,at least about 0.025 kmol/hr carbonylation catalyst, at least about 0.04kmol/hr carbonylation catalyst, at least about 0.05 kmol/hrcarbonylation catalyst, at least about 0.056 kmol/hr carbonylationcatalyst, at least about 0.1 kmol/hr carbonylation catalyst, at leastabout 0.25 kmol/hr carbonylation catalyst, at least about 0.4 kmol/hrcarbonylation catalyst, at least about 0.5 kmol/hr carbonylationcatalyst, or at least about 0.56 kmol/hr carbonylation catalyst. In someembodiments, the mass fraction of carbonylation catalyst in the recycledcarbonylation catalyst stream can be at least about 0.002, at leastabout 0.015, at least about 0.02, or at least about 0.022. In someembodiments, the mole fraction of carbonylation catalyst in the recycledcarbonylation catalyst stream can be at least about 0.0002, at leastabout 0.0015, at least about 0.002, at least about 0.003, at least about0.004, or at least about 0.005.

In some embodiments, the inlet to the carbonylation reaction system canreceive solvent from solvent feed 1424 at least about 10000 kg/hr, atleast about 11000 kg/hr, at least about 12000 kg/hr, at least about12250 kg/hr, at least about 13000 kg/hr, at least about 25000 kg/hr, atleast about 50000 kg/hr, at least about 100000 kg/hr, at least about110000 kg/hr, at least about 120000 kg/hr, at least about 122500 kg/hr,or at least about 130000 kg/hr. In some embodiments, the inlet to thecarbonylation reaction system can receive solvent from a solvent feed atleast about 150 kmol/hr, at least about 160 kmol/hr, at least about 170kmol/hr, at least about 180 kmol/hr, at least about 190 kmol/hr, atleast about 500 kmol/hr, at least about 1000 kmol/hr, at least about1500 kmol/hr, at least about 1600 kmol/hr, at least about 1700 kmol/hr,at least about 1800 kmol/hr, or at least about 1900 kmol/hr In someembodiments, the amount of solvent in the solvent feed to thecarbonylation reaction system can be fixed to ensure the residence timein the carbonylation reaction system is at a set time. For example, theresidence time can be about 1-500 minutes, about 20-450 minutes, about30-300 minutes, about 35-200 minutes, or about 40-80 minutes. Aspreviously discussed, in some embodiments, the solvent introduced to thecarbonylation reaction system can include some recycled solvents fromthe carbonylation catalyst isolation system and the BPL purificationsystem. Accordingly, in some embodiments, the inlet to the carbonylationreaction system can also receive carbon monoxide (in about 0.1-10 kg/hr,about 0.5-5 kg/hr, about 0.1-10 kg/hr, about 0.1-50 kg/hr, about 0.1-100kg/hr, about 0.5-50 kg/hr, at most about 50 kg/hr, at most about 10kg/hr, at most about 5 kg/hr, at most about 3 kg/hr, or at most about1.3 kg/hr), ethylene oxide (in about 40-80 kg/hr, about 50-70 kg/hr,about 40-150 kg/hr, about 40-250 kg/hr, about 50-500 kg/hr, about 50-800kg/hr, at most about 800 kg/hr, at most about 500 kg/hr, about mostabout 250 kg/hr, 80 kg/hr, at most about 70 kg/hr, or at most about 66kg/hr or a mass fraction of about 0.001-0.01, about 0.002-0.007, or mostabout 0.01, at most about 0.005), acetaldehyde (in about 1-200 kg/hr,about 1-150 kg/hr, about 1-100 kg/hr, about 1-50 kg/hr, about 1-20kg/hr, about 5-15 kg/hr, or at most about 200 kg/hr, at most about 150kg/hr, at most about 100 kg/hr, at most about 50 kg/hr, at most about 20kg/hr, at most about 15 kg/hr, or at most about 11 kg/hr or a massfraction of at most about 0.001), succinic anhydride (in about 1-100kg/hr, about 1-50 kg/hr, 1-10 kg/hr, about 1-5 kg/hr, or at most about50 kg/hr, at most about 10 kg/hr, 5 kg/hr, or at most about 3 kg/hr),bPL (in about at most 2000 kg/hr, at most about 1500 kg/hr, at mostabout 1000 kg/hr, at most about 500 kg/hr, 200 kg/hr, at most about 300kg/hr, at most about 500 kg/hr, at most about 550 kg/hr, or at mostabout 600 kg/hr, or a mass fraction of at most 0.1, at most about 0.075,at most about 0.05, or at most about 0.043), and carbonylation catalystor components thereof from the solvent feed. In some embodiments, themass fraction of solvent from the solvent feed can be at least about0.85, at least about 0.9, at least about 0.94, or at least about 0.95.In some embodiments, the mole fraction of solvent from the solvent feedcan be at least about 0.85, at least about 0.9, at least about 0.94, orat least about 0.95.

In some embodiments, the inlet to the carbonylation reaction system canreceive carbonylation catalyst from a solvent feed at least about 1000kg/hr, at least about 750 kg/hr, at least about 600 kg/hr, at leastabout 530 kg/hr, at least about 500 kg/hr, at least about 250 kg/hr, atleast about 100 kg/hr, at least about 75 kg/hr, at least about 60 kg/hr,at least about 53 kg/hr, or at least about 50 kg/hr. In someembodiments, the inlet to the carbonylation reaction system can receivecarbonylation catalyst from a solvent feed at least about 1 kmol/hr, atleast about 0.8 kmol/hr, at least about 0.75 kmol/hr, at least about0.56 kmol/hr, or at least about 0.5 kmol/hr, at least about 0.25kmol/hr, at least about 0.1 kmol/hr, at least about 0.1 kmol/hr, atleast about 0.075 kmol/hr, at least about 0.056 kmol/hr, or at leastabout 0.05 kmol/hr. In some embodiments, the mass fraction ofcarbonylation catalyst from the solvent feed can be at least about0.0002, at least about 0.002, at least about 0.003, or at least about0.004.

In some embodiments, the inlet to the carbonylation reaction system canreceive a solvent feed at a temperature between about 10-100° C.,between about 20-50° C., between about 25-45° C., between about 30-40°C., or about 36.6° C. In some embodiments, the inlet to thecarbonylation reaction system can receive a solvent feed at a pressureof at least about 50 bar, about 60-70 bar, or at least about 65 bar.

Other Feed Sources

The β-propiolactone production system/production process may furtherinclude other feed sources. For example, in one variation, theβ-propiolactone production system/production process further includes aLewis base additive source.

In some embodiments, a Lewis base additive may be added to thecarbonylation reactor. In certain embodiments, such Lewis base additivescan stabilize or reduce deactivation of the catalysts. In someembodiments, the Lewis base additive is selected from the groupconsisting of phosphines, amines, guanidines, amidines, andnitrogen-containing heterocycles. In some embodiments, the Lewis baseadditive is a hindered amine base. In some embodiments, the Lewis baseadditive is a 2,6-lutidine; imidazole, 1-methylimidazole,4-dimethylaminopyridine, trihexylamine and triphenylphosphine.

The exemplary system depicted in FIG. 14 also includes carbonylationproduct stream 1414, post-isolation carbonylation product stream 1416,BPL purified stream 1418, PPL product stream 1420, and GAA productstream 1422.

Reactor

In some embodiments, the carbonylation reaction system can include atleast one reactor for the carbonylation reaction. In some embodiments,the carbonylation system can include multiple reactors in series and/orparallel for the carbonylation reaction. In some embodiments, thereactor(s) can be a continuous reactor(s). Examples of suitablecontinuous reactors include but are not limited to tubular reactors(i.e., plug flow-type reactors), fixed bed reactors, fluid bed reactors,continuous stirred tank reactors (“CSTR”), heat exchanger reactors(e.g., shell and tube type reactor), loop reactors (e.g., Buss, jet,etc.), membrane reactors, or other reactors known to those of ordinaryskill in the art. In some embodiments, the carbonylation reaction systemincludes one or more CSTRs. All inlets and outlets to the carbonylationreaction system can include sensors that can determine the flowrate,composition (especially water and/or oxygen content), temperature,pressure, and other variables known to those of ordinary skill in theart. In addition, the sensors can be connected to control units that cancontrol the various streams (i.e., feed controls) in order to adjust theprocess based on the needs of the process determined by the sensorunits. Such control units can adjust the quality as well as the processcontrols of the system.

In some variations, the reactor in the β-propiolactone productionsystem/production process is configured to receive the catalyst,ethylene oxide and carbon monoxide in certain ratios. In someembodiments, the ratio of catalyst to ethylene oxide is selected, basedon other reaction conditions, so that the reaction proceeds in aneconomical and time-feasible manner. In some embodiments, the ratio ofcatalyst to ethylene oxide is about 1:10000 on a molar basis. In someembodiments, the molar ratio of catalyst to ethylene oxide is about1:5000, is about 1:2500, is about 1:2000, is about 1:1500, is about1:1000, is about 1:750, is about 1:500, is about 1:250, is about 1:200,is about 1:150, or is about 1:100. In some embodiments, theconcentration of the ethylene oxide is in the range between about 0.1 Mand about 5.0 M. In some embodiments, the concentration of the ethyleneoxide is in the range between about 0.5 M and about 3.0 M.

In certain embodiments, the molar ratio of carbon monoxide to ethyleneoxide in the reaction stream ranges from about 0.1:1 to about 100:1. Incertain embodiments, the molar ratio of carbon monoxide to ethyleneoxide in the reaction stream is about 50:1, is about 20:1, is about10:1, is about 5:1 or is about 1:1, or within a range including any twoof these ratios. In some embodiments, the ratio of carbon monoxide toethylene oxide is selected based on other reaction conditions so thatthe reaction proceeds in an economical and time-feasible manner.

In some variations, the reactor in the β-propiolactone productionsystem/production process is configured to further receive one or moreadditional components. In certain embodiments, the additional componentscomprise diluents which do not directly participate in the chemicalreactions of ethylene oxide. In certain embodiments, such diluents mayinclude one or more inert gases (e.g., nitrogen, argon, helium and thelike) or volatile organic molecules such as hydrocarbons, ethers, andthe like. In certain embodiments, the reaction stream may comprisehydrogen, carbon monoxide of carbon dioxide, methane, and othercompounds commonly found in industrial carbon monoxide streams. Incertain embodiments, such additional components may have a direct orindirect chemical function in one or more of the processes involved inthe conversion of ethylene oxide to β-propiolactone and various endproducts. Additional reactants can also include mixtures of carbonmonoxide and another gas. For example, as noted above, in certainembodiments, carbon monoxide is provided in a mixture with hydrogen(e.g., Syngas).

Because the carbonylation reaction is exothermic, the reactors used caninclude an external circulation loop for reaction mass cooling. In someembodiments, the reactors can also include internal heat exchangers forcooling. For example, in the case of a shell and tube type reactor, thereactors can flow through the tube part of the reactor and a coolingmedium can flow through the shell of the reactor or vice versa. Heatexchanger systems can vary depending on layout, reactor selection, aswell as physical location of the reactor. The reactors can employ heatexchangers outside of the reactors in order to do the cooling/heating orthe reactors can have an integrated heat exchanger such as a tube andshell reactor. For example, a CSTR can utilize a layout for heatrejection by pumping a portion of the reaction fluid through an externalheat exchanger or a plug flow-type reactor can be an integrated unitthat combines the reactor and the heat exchanger into a single unit.Additional reactor/heat exchanger systems and heat management systemscan be found in U.S. Pat. Nos. 3,128,163; 4,759,313; 8,246,915, whichare hereby incorporated by reference in their entirety. In someembodiments, heat can be removed from a CSTR by using a coolant in areactor jacket, one or more internal cooling coils, lower temperaturefeeds and/or recycle streams, an external heat exchange with pump aroundloop, and/or other methods known by those of ordinary skill in the art.In some embodiments, heat can be removed from a plug flow type reactoror a loop reaction by using a coolant in the reactor jacket and/orinternal cooling coils. Furthermore, the reaction can occur on the tubeside or the shell side of a shell and tube reactor and the other sidecan have the cooling medium. In addition, the reactors may have multiplecooling zones with varying heat transfer areas and/or heat transferfluid temperatures and flows.

The type of reactor employed and the type of heat exchanger employed(either external or integrated) can be a function of various chemistryconsiderations (e.g., reaction conversions, by-products, etc.), degreeof exotherm produced, and the mixing requirements for the reaction.

Since carbonylation reactions are exothermic reactions and the BPLpurification system and thermolysis requires energy, it is possible tointegrate at least some of the components between the carbonylationreaction system and the BPL purification system and/or thermolysissystem. For example, steam or tempered water or other appropriate heattransfer media can be produced in a heat exchanger of the carbonylationreaction system and transported to the BPL purification system forheating a distillation column for example. In addition, the BPLpurification system and the carbonylation reaction system may beintegrated into a single system or unit so that the heat produced fromthe carbonylation reaction can be used in the BPL purification system(in an evaporator or distillation column). The steam can be generated ina heat exchanger (e.g., shell and tube heat exchanger, reactor's coolingjacket, etc) via a temperature gradient between reaction fluids andwater/steam of the heat exchanger. Steam can be used for heatintegration between exothermic units (carbonylation reaction,polymerization reaction) and endothermic units (BPL purificationsystem's columns/evaporators and thermolysis reaction). In someembodiments, steam is only used for heat management and integration andwill not be introduced directly into the production processes.

As previously described, water and oxygen can damage the carbonylationcatalyst. As such, oxygen and water intrusion into the carbonylationsystem should also be minimized. As such, the reactor seals may utilizea magnetic drive, a double mechanical seal, and/or materials ofconstruction that are compatible with the reactants and products of thecarbonylation reaction but not permeable to atmosphere. In someembodiments, the materials of construction of the reactor includemetals. In some embodiments, the metals can be stainless steel. In someembodiments, the metals can be carbon steel. In some embodiments, themetals can be metal alloys such as nickel alloys. In some embodiments,the metals are chosen when compatibility or process conditions dictate,e.g., high chloride content or if carbon steel catalyzes EOdecomposition. In some embodiments, everything up until thepolymerization reaction system can include carbon steel. One of thebenefits of carbon steel over stainless steel is its cost. In someembodiments, the metals can have a surface finish so as to minimizepolymer nucleation sites. The materials of construction of the reactorcan also include elastomer seals. In some embodiments, the elastomerseals are compatible with the reactants and products of thecarbonylation reaction but not permeable to the atmosphere. Examples ofelastomer seals include but are not limited to Kalrez 6375, Chemraz 505,PTFE-encapsulated Viton, and PEEK. The materials of construction ofexternal parts of the carbonylation reaction system can be compatiblewith the environment, for example, compatible with sand, salty water,not heat absorbing, and can protect the equipment from the environment.

In some embodiments, the carbonylation reaction system is operated so asto minimize or mitigate PPL and polyethylene oxide formation prior tothe polymerization reaction system. In some embodiments, thecarbonylation reaction system is operated so as to avoid catalystdecomposition.

In some embodiments, the carbonylation reactor(s) can have a downstreamflash tank with a reflux condenser to separate unreacted carbon monoxideas a recycled carbon monoxide stream from the carbonylation reactionsystem. As previously described, the recycled carbon monoxide stream canbe sent to a CO compressor and/or combined with a fresh carbon monoxidefeed prior to being sent back into the carbonylation reaction system.The flash tank can separate most of the CO to avoid its separationdownstream, especially in the carbonylation catalyst isolation system.In some embodiments, excess gas is removed or purged from the reactoritself and thus a flash tank is not necessary.

In some embodiments, the carbonylation reactor(s) can operate at atemperature of about 40-100° C., about 50-90° C., about 60-80° C., about65-75° C., or about 70° C. In some embodiments, the reaction temperaturecan range from between about −20° C., to about 600° C. In someembodiments, the reaction temperature is about −20° C., about 0° C.,about 20° C., about 40° C., about 60° C., about 80° C., about 100° C.,about 200° C., about 300° C., about 400° C., about 500° C. or about,about 600° C. In some embodiments, the temperature is in a range betweenabout 40° C. and about 120° C. In some embodiments, the temperature isin a range between about 60° C. and about 140° C. In some embodiments,the temperature is in a range between about 40° C. and about 80° C. Insome embodiments, the temperature is in a range between about 50° C. andabout 70° C. In some embodiments, the reactants, catalyst and solventare supplied to the reactor at standard temperature, and then heated inthe reactor. In some embodiments, the reactants are pre-heated beforeentering the reactor.

In some embodiments, the carbonylation reactor(s) can operate at apressure of about 600-1200 psig, about 700-1100 psig, about 800-1000psig, about 850-950 psig, or about 900 psig. In some embodiments, thereaction pressure can range from between about 50 psig to about 5000psig. In some embodiments, the reaction pressure is about 100 psig,about 200 psig, about 300 psig, about 400 psig, about 500 psig, about600 psig, about 700 psig, about 800 psig, about 900 psig, or about 1000psig. In some embodiments, the pressure ranges from about 50 psig toabout 2000 psig. In some embodiments, the pressure ranges from about 100psig to 1000 psig. In some embodiments, the pressure ranges from about200 psig to about 800 psig. In some embodiments, the pressure rangesfrom about 800 psig to about 1600 psig. In some embodiments, thepressure ranges from about 1500 psig to about 3500 psig. In someembodiments, the pressure ranges from about 3000 psig to about 5500psig. In some embodiments, the reaction pressure is supplied entirely bythe carbon monoxide. For example, carbon monoxide is added to thereactor at high pressure to increase pressure to the reaction pressure.In some embodiments, all reactants, solvent and catalyst are supplied tothe reactor at reaction pressure.

In some embodiments, the reaction is maintained for a period of timesufficient to allow complete, near complete reaction of the ethyleneoxide to carbonylation products or as complete as possible based on thereaction kinetics and or reaction conditions. In some embodiments, thereaction time is a residence time in the carbonylation reactor in step(a). In certain embodiments, the residence time is about 12 hours, about8 hours, about 6 hours, about 3 hours, about 2 hours or about 1 hour. Incertain embodiments, the residence time is about 30 minutes, about 20minutes, about 15 minutes, about 10 minutes, about 5 minutes, about 3minutes, about 2 minutes, or about 1 minute. In certain embodiments, theresidence time is less than 1 minute.

The chemistry involved in a carbonylation reaction system can include,but are not limited to, the following three reactions: (1) CO+EO→bPL;(2) EO→acetaldehyde; (3) bPL→succinic anhydride. The conversions for thethree reactions may vary depending on many factors including amount ofreactants, amount of catalyst, temperature, pressure, flow rate, etc.However, the first reaction can have an EO conversion of about0.2-0.999, about 0.5-0.95, about 0.6-0.9, about 0.7-0.8, or about 0.75.The second reaction can have an EO conversion of about 0-0.1, about0.001-0.02, about 0.002-0.01, or about 0.005. The third reaction canhave a bPL conversion of about 0.0002-0.02, about 0.0005-0.01, about0.001-0.003, or about 0.002.

FIG. 15 illustrates an exemplary embodiment of a carbonylation reactionsystem disclosed herein. Carbonylation reaction system 1513 can includecarbonylation reaction system inlet 1509 for carbonylation reactor 1525.As previously described, the inlet can be made up of multiple inlets orfeeds into the reaction system. In addition, carbonylation reactionsystem 1513 includes flash tank 1526 with condenser 1527. Flash tank1526 and condenser 1527 separate the reactor product stream intorecycled carbon monoxide stream 1510 and carbonylation product stream1514.

Carbonylation Product Stream (i.e., BPL Product Stream)

In some embodiments, the carbonylation product stream includes at leastabout 2000 kg/hr bPL, at least about 2500 kg/hr bPL, at least about 3000kg/hr bPL, at least about 3500 kg/hr bPL, at least about 3638 kg/hr bPL,at least about 4000 kg/hr bPL, at least about 8000 kg/hr bPL, at leastabout 12000 kg/hr bPL, at least about 16000 kg/hr bPL, at least about20000 kg/hr bPL, at least about 25000 kg/hr bPL, at least about 30000kg/hr bPL, at least about 35000 kg/hr bPL, at least about 36380 kg/hrbPL, or at least about 40000 kg/hr bPL. In some embodiments, thecarbonylation product stream includes between about 2000 kg/hr bPL andabout 4000 kg/hr bPL, about 2500 kg/hr bPL and about 4000 kg/hr bPL,about 3000 kg/hr bPL and about 4000 kg/hr bPL, about 3500 kg/hr bPL andabout 4000 kg/hr bPL, about 3638 kg/hr bPL and about 4000 kg/hr bPL,between about 2000 kg/hr bPL and about 40000 kg/hr bPL, about 2500 kg/hrbPL and about 40000 kg/hr bPL, about 3000 kg/hr bPL and about 40000kg/hr bPL, about 3500 kg/hr bPL and about 40000 kg/hr bPL, about 3638kg/hr bPL and about 40000 kg/hr bPL, about 4000 kg/hr bPL and about40000 kg/hr bPL, about 8000 kg/hr bPL and about 40000 kg/hr bPL, about12000 kg/hr bPL and about 40000 kg/hr bPL, about 16000 kg/hr bPL andabout 40000 kg/hr bPL, about 20000 kg/hr bPL and about 40000 kg/hr bPL,about 25000 kg/hr bPL and about 40000 kg/hr bPL, about 30000 kg/hr bPLand about 40000 kg/hr bPL, or about 35000 kg/hr bPL and about 40000kg/hr bPL.

In some embodiments, the carbonylation product stream includes at leastabout 30 kmol/hr bPL, at least about 40 kmol/hr bPL, at least about 45kmol/hr bPL, at least about 50 kmol/hr bPL, at least about 55 kmol/hrbPL, at least about 100 kmol/hr bPL, at least about 200 kmol/hr bPL, atleast about 300 kmol/hr bPL, at least about 400 kmol/hr bPL, at leastabout 450 kmol/hr bPL, at least about 500 kmol/hr bPL, or at least about550 kmol/hr bPL. In some embodiments, the mass fraction of bPL in thecarbonylation product stream can be about 0.1-0.4, about 0.15-0.3, about0.18-0.25, about 0.2-0.23, at least about 0.15, at least about 0.2, orat least about 0.224. In some embodiments, the mole fraction of bPL inthe carbonylation product stream can be about 0.1-0.4, about 0.15-0.3,about 0.18-0.25, about 0.21-0.23, at least about 0.15, at least about0.2, or at least about 0.22. The carbonylation product stream can alsoinclude other components including unreacted ethylene oxide (in massfraction of about 0.005-0.05, about 0.02-0.045, about 0.04, at mostabout 0.014, at most about 0.02, or at most about 0.05), unreactedcarbon monoxide (in mass fraction of about 0.0005-0.01, at most about0.01, or at most about 0.02), acetaldehyde (in mass fraction of about0.0005-0.001, at most about 0.001, or at most about 0.002), succinicanhydride (in mass fraction of about 0.0005-0.001, at most about 0.001,or at most about 0.002), carbonylation catalyst (in about 40-640 kg/hr,about 45-600 kg/hr, about 50-600 kg/hr, about 50-300 kg/hr, about 50-100kg/hr, about 40-64 kg/hr, about 45-60 kg/hr, about 50-60 kg/hr, at most54.8 kg/hr, at most about 60 kg/hr, at most 300 kg/hr, or at most 600kg/hr or a mass fraction of about 0.001-0.005, about 0.002-0.004, atmost about 0.003, or at most about 0.004), and the remainder solvent. Insome embodiments, the carbonylation product stream can includesufficient ethylene oxide so as to prevent anhydride formation.

In some embodiments, the carbonylation product stream from thecarbonylation reaction system can have a temperature of about 50-100°C., about 60-90° C., about 65-75° C., or about 70° C. In someembodiments, the carbonylation product stream can have a pressure ofabout 1-5 bar, about 2-4 bar, or about 3 bar.

In some embodiments, the carbonylation reaction system has a selectivityof at least about 95%, at least about 97%, at least about 99%, at leastabout 99.5%, or at least about 99.8%. In some embodiments, thecarbonylation reaction system has a yield of at least about 90%, atleast about 95%, at least about 98%, at least about 99%, or at leastabout 99.5%. In some embodiments, the selectivity of bPL is the ratio ofbPL yield to ethylene oxide conversion, wherein the bPL yield ismeasured relative to ethylene oxide. In other embodiments, theselectivity of bPL is the ratio of bPL yield to carbon monoxideconversion, wherein the bPL yield is measured relative to carbonmonoxide.

Carbonylation Catalyst Recycle System

With reference again to FIG. 1, the carbonylation catalyst recyclesystem may be employed to recover at least a portion of thecarbonylation catalyst, or components thereof, present in theβ-propiolactone product stream. Such recovered carbonylation catalystmay be recycled and reused in the β-propiolactone productionsystem/production process.

Carbonylation catalyst components may include, for example, compoundsproduced by degradation of the catalyst, compounds used to produce thecatalyst, metals or metal ions which were part of the catalyst, anyorganic compounds which were part of the catalyst, metal carbonyls ormetal complexes which were part of the catalyst. For example, in someembodiments, carbonylation catalyst components are carbonyl cobaltate,aluminum salen compounds, aluminum porphyrin compounds, aluminumsalophen compounds, cobalt or cobalt ions, or aluminum or aluminum ions,or any combinations thereof.

Any suitable methods and techniques known in the art may be used torecover at least a portion of the carbonylation catalyst present in theβ-propiolactone product stream. Such methods and techniques may include,for example, nanofiltration (as depicted in FIG. 1), distillation,liquid-liquid extraction, ionic liquids, and ion exchange, oradsorption. Combinations of methods and techniques described herein mayalso be employed.

Nanofiltration

In some embodiments, the carbonylation catalyst recycle system involvesthe use of nanofiltration. For example, a nanofiltration membrane may beused. In some variations, the nanofiltration membrane is an organicsolvent-stable nanofiltration membrane. Although any nanofiltrationmembrane may be used in combination with any organic solvent or organicsolvent system compatible with the carbonylation reaction, thenanofiltration membrane may be selected in combination with the organicsolvent or solvents such that the process achieves predetermined levelsof lactone formation and catalyst-lactone separation. In somevariations, the nanofiltration membrane is a polymeric nanofiltrationmembrane, while in other variations, the nanofiltration membrane is aceramic nanofiltration membrane.

In some embodiments, the nanofiltration membrane is a polymericmembrane. Any suitable polymeric membranes may be used in the methodsdescribed herein. For example, in some variations, the polymericmembrane comprises polyimides, polyamide-imides, silicone-coatedpolyamide composites, polyacrylonitriles, polydimethylsiloxane films onpolyacrylonitrile supports, silcones, polyphosphazenes, polyphenylenesulfide, polyetheretherketone, or polybenzimidazol. In certainvariations, the polymeric membrane has a silicone backbone.

In certain variations, the polymeric membrane is selected frompolyimides, including those marketed under the trademark STARMEM byMembrane Extraction Technology Ltd (Wembley, UK) and integrally skinnedasymmetric membranes made from polyimides, polyamide-imides,silicone-coated polyamide composites, polyacrylonitriles,polydimethylsiloxane films on polyacrylonitrile supports, silcones,polyphosphazenes, polyphenylene sulfide, polyetheretherketone, andpolybenzimidazol. In some embodiments, the organic solvent istetrahydrofuran and the nanofiltration membrane is an integrally skinnedasymmetric polyimide membrane made from Lenzing P84 or a ST ARMEM®polyimide membrane. In some embodiments, the organic solvent is diethylether and the nanomembrane is a silicone-coated polyamide composite. Insome embodiments, the nanofiltration membrane is a commerciallyavailable membrane. In other embodiments, the nanofiltration membrane isan integrally skinned asymmetric polyimide membrane made from LenzingP84 and manufactured by GMT Membrantechnik GmbH (Rheinfelden, Germany).In some other embodiments, the nanofiltration membrane is a STARMEM®polyimide membrane from Membrane Extraction Technology Ltd (Wembley, UK)and the nanofiltration step is performed at a temperature under 50° C.and a pressure under 60 bar. In still other embodiments, thenanofiltration membrane is a silicone-coated organic solvent resistantpolyamide composite nanofiltration membrane as disclosed in U.S. Pat.No. 6,887,380, incorporated herein by reference. In other variations,the nanofiltration membrane is a ceramic membrane comprising inorganicmaterials.

Nanofiltration membranes of various configurations may be employed inthe carbonylation catalyst recycling system. For example, in someembodiments, the membrane is a plate-and-frame membrane. With referenceto FIG. 3, exemplary carbonylation catalyst recycle system 300 that usesmembrane 310 is depicted. Feed 302 may include, for example,β-propiolactone, carbonylation solvent, small amounts of ethylene oxideand carbon monoxide, carbonylation catalyst, and by-products (such asacetaldehyde and succinic anhydride). Feed 302 is transferred tomembrane via pumps 306 and 308. Sensor 304 is positioned before pump 306to regulate the rate at which feed 302 is pumped through membrane 310.In some variations, sensor 304 may be a ultra-violet (UV) sensor. Othersuitable sensors may also be employed. Feed 302 passes through membrane310 by way of the transmembrane pressure, varied according to the pumpset points. In some variations, membrane 310 is a plate-and-framemembrane, as depicted in FIG. 3. However, in other variations, othersuitable membranes may be used. For example, in other variation,membrane 310 of carbonylation catalyst recycle system 300 may be aspiral wound membrane or a tubular membrane, and such alternativeconfigurations are discussed in further detail below.

With reference again to FIG. 3, membrane 310 produces permeate stream316 and retentate stream 324. Permeate stream 316 may include, forexample, β-propiolactone, carbonylation solvent, small amounts ofethylene oxide and carbon monoxide, by-products (such as acetaldehydeand succinic anhydride), and trace amounts of carbonylation catalyst.Further, permeate stream 316 may have a permeability of at least 0.5L/m² hr bar, at least 0.6 L/m² hr bar, at least 0.7 L/m² hr bar, atleast 0.8 L/m² hr bar, at least 0.9 L/m² hr bar, at least 1.0 L/m² hrbar, at least 1.1 L/m² hr bar, at least 1.2 L/m² hr bar, at least 1.3L/m² hr bar, at least 1.4 L/m² hr bar, at least 1.5 L/m² hr bar, atleast 1.6 L/m² hr bar, at least 1.7 L/m² hr bar, at least 1.8 L/m² hrbar, at least 1.9 L/m² hr bar, at least 2 L/m² hr bar, at least 2.5 L/m²hr bar, at least 3 L/m² hr bar, at least 3.5 L/m² hr bar, or at least 4L/m² hr bar; or between 0.5 L/m² hr bar and 5 L/m² hr bar, or between 3L/m² hr bar and 4.5 L/m² hr bar; or between 0.5 L/m² hr bar and 10 L/m²hr bar, or between 3 L/m² hr bar and 10 L/m² hr bar. In some variations,permeability (or membrane permeability) refers to volumetric flow rateof material that permeates through a specified surface area at aspecified transmembrane pressure (TMP). In some variations, thetransmembrane pressure is the pressure difference between the retentateside of the membrane and the permeate side of the membrane. In someembodiments, the relationship can be expressed asPermeability=Volumetric flow rate/(Surface Area×TMP). In someembodiments, permeability may be determined by measuring the flow rateof material which permeates across a membrane sample of known surfacearea at a known TMP.

Sensor 312 is positioned after membrane 310 to analyze the contents ofpermeate stream 316. In some variations, sensor 312 may be a UV sensor.Other suitable sensors may also be employed.

Carbonylation catalyst recycle system 300 is configured to achieve acatalyst rejection of at least 80%, at least 85%, at least 90%, at least91%, at least 92%, at least 93%, at least 94%, at least 95%, at least96%, at least 97%, at least 98%, at least 99%, at least 99.1%, at least99.2%, at least 99.3%, at least 99.4%, at least 99.5%, at least 99.6%,at least 99.7%, at least 99.8%, or at least 99.9%, or 100%. In somevariations, catalyst rejection refers to the percentage (by mass) ofcatalyst which permeates through the membrane compared to that whichdoes not and is retained on the retentate side of the membrane. Catalystrejection may be determined by any suitable method in the art,including, for example, using analytical instruments to detect catalystconcentrations at the membrane feed, permeate and retentate.

With reference to FIG. 3, pressure control valve 314 is positioned aftersensor 312 and biased to upstream flash units. In some embodiments,pressure control valve (PCV) 314 can be used to control transmembranepressure (TMP) which may affect performance of the membrane. Sensor 312may detect catalyst rejection and provide a feedback signal to PCV 314to make adjustments for system performance. PCV 314 may in someembodiments detect the pressure of the upstream flash tank and preventvolatile species (for example, carbon monoxide) from vaporizing aspressure changes across the membrane. Vaporization or flashing acrossthe membrane may affect the durability of the membrane.

Retentate stream 324 may include, for example, carbonylation solvent,β-propiolactone, and carbonylation catalyst. Pump 322 may be used totransfer retentate stream 324 to the β-propiolactone productionsystem/production process described herein (e.g., to a carbonylationreactor of the β-propiolactone production system/production process). Insome embodiments, catalyst may deactivate as it is circulated throughthe membrane system on the retentate side (for example, with exposure tooxygen or water). In certain embodiments, a portion of the retentatestream is purged for a period of time to avoid accumulation ofdeactivated catalyst within the system. Valve 320 is configured to purgethe system and bleed 326.

As discussed above, while FIG. 3 depicts the use of a plate-and-framemembrane, other membrane configurations may be employed. For example, inother embodiments, the membrane is a spiral wound membrane. In yet otherembodiments, the membrane is a tubular membrane. In still otherembodiments, the membrane is a pleated sheet membrane.

In one variation, the membrane is a polymeric membrane in a plate andframe configuration. In another variation, the membrane is a polymericmembrane in a spiral wound configuration. In yet another variation, themembrane is a ceramic membrane in a tubular configuration.

While FIG. 3 depicts the use of one membrane, in other variations, aplurality of membranes may be used. For example, at least two membranesconnected in series may be used. In one variation, a plurality ofplate-and-frame membranes connected in series may be used. In othervariations, a plurality of spiral wound membranes connected in seriesmay be used. In other variations, a plate-and-frame membrane may beconnected in series with a spiral wound membrane. It should beunderstood that the membrane configurations may be in series, inparallel, or in a combination of series and parallel. For example, insome embodiments, the membranes are configured in a “Christmas tree”configuration.

In one embodiment, the nanofiltration membrane is a polymeric, spiralwound membrane with a silicone backbone, carbonylation catalystrejection rate of at least 99%, and permeability of at least 1 L/m² hrbar.

Distillation

In other embodiments, the carbonylation catalyst recycle system involvesa distillation apparatus.

In some variations, the distillation apparatus recover at least aportion of the carbonylation catalyst present in the β-propiolactoneproduct stream using a multi-solvent system. For example, in onevariation, a two-solvent system may be used, wherein the first solventhas a boiling point above 166° C. and may serve as the carrier of thecatalyst, and the second solvent is selected to facilitate thecarbonylation reaction.

In other variations, the distillation may include heating theβ-propiolactone product stream to volatilize at least a portion of theβ-propiolactone and/or the solvent to form a distillate, removing thedistillate, and condensing the distillate. In other embodiments, thedistillation is a vacuum distillation, wherein the distillate is formedby reducing the pressure of the β-propiolactone product stream. Incertain embodiments, vacuum distillation allows at least a portion ofthe carbonylation catalyst to be removed from the β-propiolactoneproduct stream without degradation of the catalyst at highertemperatures. In other variations, the distillation is performed by bothincreasing the temperature and decreasing the pressure of theβ-propiolactone product stream. The carbonylation catalyst remaining thein the retained mixture after distillation can then be isolated forreuse in the carbonylation reaction using any methods known in the art,including, for example, solvent-solvent extraction, nanofiltration,ionic liquids, or adsorption.

Liquid-Liquid Extraction

In other embodiments, the carbonylation catalyst recycle system involvesa liquid-liquid extraction apparatus.

In some variations, the liquid-liquid extraction apparatus employs anextraction solvent in which the catalyst (or a component of thecatalyst) is soluble or at least partially soluble. In other variations,the extraction solvent is one in which the β-propiolactone is soluble orat least partially soluble, but which has little tendency to dissolvethe carbonylation catalyst (or one or more components of thecarbonylation catalyst). In either case, the use of the extractionsolvent results in the formation of two phases. In certain embodiments,the extraction solvent is a highly polar solvent such as water or anionic liquid. In certain embodiments, the extraction solvent issupercritical CO₂. In certain embodiments, the extraction solvent iswater or an aqueous solution. In certain embodiments, the extractionsolvent is an ionic liquid. In certain embodiments where the solvent isan ionic liquid, the ionic liquid has a formula [Cat⁺][X″] wherein[Cat⁺] refers to one or more organic cationic species; and [X″] refersto one or more anions. In certain embodiments, [Cat⁺] is selected fromthe group consisting of: ammonium, tetralkylammonium, benzimidazolium,benzofuranium, benzothiophenium, benzotriazolium, borolium, cinnolinium,diazabicyclodecenium, diazabicyclononenium,1,4-diazabicyclo[2.2.2]octanium, diazabicyclo-undecenium, dithiazolium,furanium, guanidinium, imidazolium, indazolium, indolinium, indolium,morpholinium, oxaborolium, oxaphospholium, oxazinium, oxazolium,iso-oxazolium, oxothiazolium, phospholium, phosphonium, phthalazinium,piperazinium, piperidinium, pyranium, pyrazinium, pyrazolium,pyridazinium, pyridinium, pyrimidinium, pyrrolidinium, pyrrolium,quinazolinium, quinolinium, iso-quinolinium, quinoxalinium,quinuclidinium, selenazolium, sulfonium, tetrazolium, thiadiazolium,iso-thiadiazolium, thiazinium, thiazolium, iso-thiazolium, thiophenium,thiuronium, triazinium, triazolium, iso-triazolium, uronium, and anycombination of two or more of these. In accordance with the presentinvention, [X″] may comprise an anion selected from halides, sulphates,sulfonates, sulfonimides, phosphates, phosphonates, carboxylates, CN⁻,NO₃ ⁻, NO₂ ⁻, BF₄ ⁻ and PF₆ ⁻.

In some embodiments, the extraction solvent includes pentane,cyclohexane, hexane, heptane, tetrahydrofuran, p-dioxane,4-methyl-1,3-dioxolan-2-one, N,N-dimethylformamide,1-methyl-2-pyrrolidinone, or sulfolane, or any combinations thereof. Inone embodiment, the extraction solvent includes sulfolane and hexane. Inanother embodiment, the liquid-liquid extraction solvent includessulfolane, hexane, and dioxane.

Precipitation

In certain embodiments, the carbonylation catalyst recycle system isconfigured to precipitate the carbonylation catalyst. Precipitation ofthe carbonylation catalyst may be accomplished by any known methods andtechniques. Suitable means of precipitating the catalyst will beapparent to the skilled chemist and may include, but are not limited to:adding a solvent to the β-propiolactone product stream in which thecatalyst (or a component thereof) is poorly soluble, cooling theβ-propiolactone product stream, adding a material that interacts withthe catalyst (or a component thereof) to form an insoluble adduct,removing solvent, excess feedstock, or carbon monoxide from theβ-propiolactone product stream, and combinations of any two or more ofthese. In certain embodiments where the step of treating theβ-propiolactone product stream to separate a portion of thecarbonylation catalyst entails precipitation, the precipitation stepcomprises adding a solvent in which the catalyst (or a component of thecatalyst) is poorly soluble. In certain embodiments, a non-polar solventsuch as an aliphatic hydrocarbon, an aromatic hydrocarbon, or condensedphase CO₂ is added to precipitate the catalyst. In certain embodiments,a solvent selected from butane, pentane, hexane, heptane, octane,cyclopentane, cyclohexane, decalin, higher alkanes, and mixtures of twoor more alkanes is added to the β-propiolactone product stream toprecipitate the catalyst or a catalyst component. In certainembodiments, a solvent selected from benzene, toluene, xylene,mesitylene, chlorobenzene, or other substituted benzene compounds isadded to the β-propiolactone product stream to precipitate the catalystor a catalyst component. In certain embodiments, supercritical CO₂ isadded to the β-propiolactone product stream to precipitate the catalystor a catalyst component. In certain embodiments where the carbonylationcatalyst comprises the combination of a Lewis acidic metal complex and ametal carbonyl compound and a non-polar solvent is added to theβ-propiolactone product stream, this causes precipitation of the Lewisacidic metal complex but leaves at least a portion of the metal carbonylcomponent of the catalyst behind in the β-propiolactone product stream.In embodiments where the catalyst is precipitated, the step ofseparating the carbonylation catalyst typically includes further stepsto remove the precipitate from the product stream, such isolation stepsare well known in the art and can include, but are not limited tofiltration, sedimentation, centrifugation, coagulation, and combinationsof two or more of these.

Adsorption

In certain embodiments, the carbonylation catalyst recycle system isconfigured to separate the carbonylation catalyst by adsorbing thecarbonylation catalyst or components thereof. In some variations,adsorption can entail treating the product streams containingcarbonylation catalyst with a solid adsorbing material. Suitable solidadsorbing materials may include inorganic substances, activated carbon,polymers, resins, or any combination of two or more of these. Suitableinorganic adsorbing materials may include silica gel, silicate minerals,clays, diatomaceous earth, Fuller's earth, ceramics, zirconias,molecular sieves and the like. Suitable polymers may includepolystyrenes, polyacrylonitrile, polyimides, polyolefins, polyesters,polyethers, polycarbonates, polyisocyanates, and the like. Such polymersmay optionally include additional chemical functional groups to enhancetheir ability to adsorb carbonylation catalysts or catalyst components.Such functional groups may include acids (e.g., sulfonic or carboxylicacids), coordinating groups (e.g., amine, thiol, phosphine, nitrile, orboron groups), and/or bases, (e.g., amine groups or nitrogenheterocycles). In certain cases, the adsorbing materials (e.g., whetherinorganic or polymeric) are acidic, basic, or have undergone chemicaltreatments to enhance the affinity of the catalyst. In embodiments wherecarbonylation catalyst is removed from the product streams containingcarbonylation catalyst by adsorption, the adsorbent can be contactedwith the product stream by any conventional method. This includes, butis not limited to: flowing the product streams containing carbonylationcatalyst through a fixed bed of adsorbent; flowing the product streamscontaining carbonylation catalyst through a fluidized bed of adsorbent;flowing the product streams containing carbonylation catalyst throughfabrics, meshes, or filtration plates comprising the adsorbent material;or slurrying the product streams containing carbonylation catalyst withthe adsorbent material (typically followed by filtration,centrifugation, sedimentation or the like to remove the adsorbent fromthe product stream).

In embodiments where the β-propiolactone product stream is flowedthrough a column of adsorbent, it may be desirable to provide aplurality of such columns in parallel with a provision to switch theflow from one column to another. Thus when one column of adsorbentbecomes saturated with catalyst, it can be switched out of the flow pathand the flow diverted to a fresh column—in certain embodiments, theinterval of time from when a column is placed in the flow path to whenit is switched out of the flow path corresponds to the “first timeinterval” recited in the methods described herein. Where an adsorbent isused to remove catalyst from the β-propiolactone product stream, theinventive methods will typically include a step of desorbing thecatalyst or catalyst component(s) from the adsorbent. Such desorptionmethods are well known in the art and will vary depending on theidentity of the adsorbant and the catalyst. Desorption can includetreating with a polar solvent or solute which displaces the catalyst orcatalyst component, or can comprise a reactive process where a reagentis added to the adsorbed catalyst to regenerate it or form a specieswhich is less adhered to the adsorbing solid.

Ion Exchange

In certain embodiments, the carbonylation catalyst recycle system may beconfigured to separate the carbonylation catalyst by ion exchange of thecarbonylation catalyst or components thereof. In certain embodiments,the carbonylation catalyst recycle system is configured to separate thecarbonylation catalyst by treating the β-propiolactone product streamwith ion exchange materials. The ion exchange materials may be, forexample, cationic, anionic, amphoteric, Lewis basic, Lewis acidic, ormay comprise chelating groups. In certain embodiments, the ion exchangematerial may be a cation exchanger. In certain embodiments, functionalgroups on the cation exchange materials may be selected from: —SO₃, PO₃²⁻, —COOH, —C₆H₄OH, —SH, —AsO₃, or —SeO₃, or combinations of two or moreof these. In certain embodiments, functional groups on the cationexchange materials comprise —SO₃

In certain embodiments, the ion exchange material may be an anionexchanger. In certain embodiments, functional groups on the anionexchange materials may be selected from: —N⁺(alkyl)₃, —N⁺(CH₃)₃,—N⁺(CH₃)₂C₂H₄OH, —N⁺(CH₃)₂C₂H₅, —P⁺(alkyl)₃, —P⁺(aryl)₃, —P⁺(C₄H₉)₃, or—P⁺(Ph)₃, or combinations of two or more of these. In certainembodiments, functional groups on the anion exchange materials comprise—N⁺(alkyl)₃. In certain embodiments, functional groups on the anionexchange materials comprise —P⁺(alkyl)₃. In certain embodiments,functional groups on the anion exchange materials comprise —P⁺(aryl)₃.

In certain embodiments, the carbonylation catalyst recycle system isconfigured to separate the carbonylation catalyst by anion exchange andcation exchange. In certain embodiments, where the carbonylationcatalyst comprises the combination of a cationic Lewis acid and ananionic metal carbonyl, each is removed separately and the methodcomprises treating the β-propiolactone product stream with a cationexchange material to remove the Lewis acid and an anion exchangematerial to remove the metal carbonyl. In certain embodiments the anionand cation exchange are performed concomitantly. In certain embodiments,the anion and cation exchange are performed sequentially. In certainembodiments, the anion exchange is performed first followed by cationexchange. In certain embodiments, the cation exchange is performed firstfollowed by anion exchange. In certain embodiments, an ion exchangematerial used in the separation step comprising an organic ion exchangeresin may prove useful. Organic ion exchange resins generally possess athree dimensional structure, the matrix. Functional groups maybeattached to the structure, or directly incorporated in the polymericchains. The matrix may be constructed from linear polymeric chainscross-linked with each other by relatively short links. By way ofexample, in various aspects, the present disclosure includes the use ofion exchange materials comprised of sulphonated polystyrene cross-linkedwith divinylbenzene:

In various aspects, ion exchange materials may take the form of gels, orgel resins, distributed across a bead, or other support substrate. Invarious aspects, ion exchange materials may take the form of macroporousresins which have a heterogeneous structure consisting of two phases, agel region comprised of polymers and macroscopic permanent pores. Invarious embodiments of the present disclosure, the ion exchangematerials comprise macroreticular resins which are additionallymacroporous resins in which the gel regions consist of a plurality ofbead micro-grains. Ion exchange materials may comprise a wide variety ofmorphologies and forms, including variations in porosity and othersurface properties. In various aspects, materials can be formed into,but not limited to beads, pellets, spheres, spheroids, rings, hollowcylinders, blocks, fibers, meshes, membranes, textiles.

In various aspects, the bead size may be widely distributed, or may bevery narrow, so-called mono-disperse resins. In embodiments wherecatalyst is removed from the β-propiolactone product stream by ionexchange, the ion exchange material can be contacted with the productstream by any conventional method. This includes, but is not limited to:flowing the β-propiolactone product stream through a fixed bed of asolid ion exchange material (i.e. in the form of beads, granules orother particles); flowing the β-propiolactone product stream through afluidized bed of adsorbent, flowing the β-propiolactone product streamthrough fabrics, meshes, or filtration plates comprising the ionexchange material, or slurrying the β-propiolactone product stream withthe ion exchange material (typically followed by filtration,centrifugation, sedimentation or the like to remove the ion exchangematerial from the product stream). In embodiments where theβ-propiolactone product stream is flowed through a packed column of ionexchange material, it may be desirable to provide a plurality of suchcolumns in parallel with a provision to switch the flow from one toanother periodically. Thus when one column of ion exchange materialbecomes saturated with catalyst, it can be switched out of the flow pathand the flow diverted to a fresh column. In certain embodiments, theinterval of time from when a column is placed in the flow path to whenit is switched out of the flow path corresponds to the “first timeinterval” recited in the methods described herein.

Where an ion exchange material is used to remove catalyst from theβ-propiolactone product stream, the inventive methods will typicallyinclude a subsequent step of removing the catalyst or catalystcomponent(s) from the ion exchange material. Such removal methods arewell known in the art and typically involve contacting the ion exchangeresin with a strong solution of a salt, the anion or cation of whichwill displace the catalyst component from the ion exchange material. Thespecifics of this removal step may vary depending on the identity of theadsorbent and the catalyst, but suitable methods are known to thoseskilled in the art.

Ionic Liquids

In certain embodiments, the carbonylation catalyst recycle system isconfigured to separate the carbonylation catalyst by using ionicliquids. For example, in some embodiments, In certain embodiments, thecarbonylation catalyst recycle system is configured to separate thecarbonylation catalyst using an ionic liquid to form a biphasic systemcomprising an ionic liquid phase and a β-propiolactone product stream.At least a portion of the catalyst (or a component thereof) is extractedinto the ionic liquid phase, such that the concentration of catalyst isreduced in the reaction product phase. The ionic liquid phase comprisingat least a portion of the carbonylation catalyst is then removed, thecarbonylation catalyst is isolated from the ionic liquid phase using anysuitable methods known in the art, and the isolated carbonylationcatalyst is recycled back into the carbonylation reactor. For example,in some embodiments the carbonylation catalyst is isolated from theionic liquid phase using, nanofiltration or precipitation. It may alsobe possible at times to use an ion exchange resin for such separation.

Any suitable ionic liquid known in the art may be used. In someembodiments, a mixture of ionic liquids is used.

Materials of Construction

The materials of construction suitable for the carbonylation catalystrecycling system may use any materials that are compatible with, forexample, the membrane used. In some variations, the carbonylationcatalyst recycling system has inert, metal surfaces, for example, toreduce or eliminate polymer nucleation sites.

In other variations, the carbonylation catalyst recycling system may useelastomer seals that are compatible with ethylene oxide, carbon monoxideand/or β-propiolactone, and has little to no permeability to atmosphere.Examples may include: Kalrez 6375, Chemraz 505, PTFE encapsulated Viton,and PEEK.

In yet other variations, the materials of construction of external partsof the carbonylation catalyst recycling system may be compatible withthe environment, including, for example, sand and salty water, and isnot heat absorbing. Further, safety interlocks and safe operatingparameters may be employed. For example, the carbonylation catalystrecycling system may be configured to mitigate polypropiolactoneformation prior to the polypropiolactone production system/productionprocess, and/or to avoid catalyst decomposition (e.g., by addition of COpressure on permeate or retentate side).

β-Propiolactone Product Stream Entering Carbonylation Catalyst RecyclingSystem

With reference again to FIG. 1, the β-propiolactone product stream fromthe β-propiolactone production system/production process is transferredto the carbonylation catalyst recycling system. In some embodiments, theβ-propiolactone product stream includes at least about 2000 kg/hr bPL,at least about 2500 kg/hr bPL, at least about 3000 kg/hr bPL, at leastabout 3500 kg/hr bPL, at least about 3638 kg/hr bPL, at least about 4000kg/hr bPL, at least about 5000 kg/hr bPL, at least about 1000 kg/hr bPL,at least about 20000 kg/hr bPL, at least about 35000 kg/hr bPL, at leastabout 36380 kg/hr bPL, or at least about 40000 kg/hr bPL. In someembodiments, the β-propiolactone product stream includes about 2000kg/hr bPL, about 2500 kg/hr bPL, about 3000 kg/hr bPL, about 3500 kg/hrbPL, about 3638 kg/hr bPL, about 4000 kg/hr bPL, about 5000 kg/hr bPL,about 1000 kg/hr bPL, about 20000 kg/hr bPL, about 35000 kg/hr bPL,about 36380 kg/hr bPL, or about 40000 kg/hr bPL. In some embodiments,the β-propiolactone product stream includes between about 2000 kg/hr bPLand 4000 kg/hr bPL, between about 2500 kg/hr bPL and 4000 kg/hr bPL,between about 3000 kg/hr bPL and 4000 kg/hr bPL, between about 3500kg/hr bPL and 4000 kg/hr bPL, between about 3638 kg/hr bPL and 4000kg/hr bPL, between about 2000 kg/hr bPL and 40000 kg/hr bPL, betweenabout 2500 kg/hr bPL and 40000 kg/hr bPL, between about 3000 kg/hr bPLand 40000 kg/hr bPL, between about 3500 kg/hr bPL and 40000 kg/hr bPL,between about 3638 kg/hr bPL and 40000 kg/hr bPL, between about 4000kg/hr bPL and 40000 kg/hr bPL, between about 5000 kg/hr bPL and 40000kg/hr bPL, between about 1000 kg/hr bPL and 40000 kg/hr bPL, betweenabout 20000 kg/hr bPL and 40000 kg/hr bPL, between about 35000 kg/hr bPLand 40000 kg/hr bPL, between about 36380 kg/hr bPL and 40000 kg/hr bPL,or between about 40000 kg/hr bPL and 40000 kg/hr bPL. In someembodiments, the β-propiolactone product stream includes at least about30 kmol/hr bPL, at least about 40 kmol/hr bPL, at least about 45 kmol/hrbPL, at least about 50 kmol/hr bPL, at least about 55 kmol/hr bPL, atleast about 100 kmol/hr bPL, at least about 200 kmol/hr bPL, at leastabout 300 kmol/hr bPL, at least about 400 kmol/hr bPL, at least about450 kmol/hr bPL, at least about 500 kmol/hr bPL, or at least about 550kmol/hr bPL. In some embodiments, the mass fraction of bPL in theβ-propiolactone product stream can be about 0.1-0.4, about 0.15-0.3,about 0.18-0.25, about 0.2-0.23, at least about 0.15, at least about0.2, or at least about 0.224. In some embodiments, the mole fraction ofbPL in the β-propiolactone product stream can be about 0.1-0.4, about0.15-0.3, about 0.18-0.25, about 0.21-0.23, at least about 0.15, atleast about 0.2, or at least about 0.22. The β-propiolactone productstream can also include other components including unreacted ethyleneoxide (in mass fraction of about 0.005-0.05, about 0.01-0.045, about0.04, at most about 0.014, at most about 0.02, or at most about 0.05),unreacted carbon monoxide (in mass fraction of about 0.0005-0.01, atmost about 0.01, or at most about 0.02), acetaldehyde (in mass fractionof about 0.0005-0.005, at most about 0.005, or at most about 0.01),succinic anhydride (in mass fraction of about 0.0005-0.005, at mostabout 0.005, or at most about 0.001), carbonylation catalyst (in about40-640 kg/hr, 300-640 kg/hr, 40-300 kg/hr, 40-64 kg/hr, about 45-60kg/hr, about 50-60 kg/hr, at most 54.8 kg/hr, at most 60 kg/hr, at most100 kg/hr, at most 300 kg/hr, or at most about 600 kg/hr or a massfraction of about 0.001-0.005, about 0.002-0.004, at most about 0.003,or at most about 0.004), and the remainder solvent. In some embodiments,the β-propiolactone product stream includes carbonylation catalystcomponents (in about 40-640 kg/hr, 300-640 kg/hr, 40-300 kg/hr, 40-64kg/hr, about 45-60 kg/hr, about 50-60 kg/hr, at most 54.8 kg/hr, at most60 kg/hr, at most 100 kg/hr, at most 300 kg/hr, or at most about 600kg/hr or a mass fraction of about 0.001-0.005, about 0.002-0.004, atmost about 0.003, or at most about 0.004).

In some embodiments, the β-propiolactone product stream from theβ-propiolactone production system/production process can have atemperature of about 40-100° C., about 50-90° C., about 65-75° C., orabout 70° C. In some embodiments, the β-propiolactone product stream canhave a pressure of about 1-15 bar, about 2-10 bar, or about 7 bar.

β-Propiolactone Product Stream Exiting Carbonylation Catalyst RecyclingSystem

In some embodiments, the β-propiolactone product stream exiting thecarbonylation catalyst recycling system includes at least about 2000kg/hr bPL, at least about 2500 kg/hr bPL, at least about 3000 kg/hr bPL,at least about 3100 kg/hr bPL, at least about 3200 kg/hr bPL, at leastabout 3500 kg/hr bPL, at least about 3638 kg/hr bPL, at least about 4000kg/hr bPL, at least about 5000 kg/hr bPL, at least about 1000 kg/hr bPL,at least about 20000 kg/hr bPL, or at least about 35000 kg/hr bPL. Insome embodiments, the β-propiolactone product stream includes about 2000kg/hr bPL, about 2500 kg/hr bPL, about 3000 kg/hr bPL, about 3500 kg/hrbPL, about 3638 kg/hr bPL, about 4000 kg/hr bPL, about 5000 kg/hr bPL,about 1000 kg/hr bPL, about 20000 kg/hr bPL, about 35000 kg/hr bPL,about 36380 kg/hr bPL, or about 40000 kg/hr bPL. In some embodiments,the β-propiolactone product stream exiting the carbonylation catalystrecycling system includes between about 2000 kg/hr bPL and 3500 kg/hrbPL, between about 2500 kg/hr bPL and 3500 kg/hr bPL, between about 3000kg/hr bPL and 3500 kg/hr bPL, between about 2000 kg/hr bPL and 35000kg/hr bPL, between about 2500 kg/hr bPL and 35000 kg/hr bPL, betweenabout 3000 kg/hr bPL and 35000 kg/hr bPL, between about 3500 kg/hr bPLand 35000 kg/hr bPL, between about 3638 kg/hr bPL and 35000 kg/hr bPL,between about 4000 kg/hr bPL and 35000 kg/hr bPL, between about 5000kg/hr bPL and 35000 kg/hr bPL, between about 1000 kg/hr bPL and 35000kg/hr bPL, or between about 20000 kg/hr bPL and 35000 kg/hr bPL. In someembodiments, the post-isolation β-propiolactone product stream includesat least about 30 kmol/hr bPL, at least about 35 kmol/hr bPL, at leastabout 40 kmol/hr bPL, at least about 43 kmol/hr bPL, at least about 45kmol/hr bPL, at least about 100 kmol/hr bPL, at least about 200 kmol/hrbPL, at least about 300 kmol/hr bPL, or at least about 350 kmol/hr bPLIn some embodiments, the mass fraction of bPL in the post-isolationβ-propiolactone product stream can be about 0.1-0.4, about 0.15-0.3,about 0.18-0.25, about 0.2-0.24, at least about 0.15, at least about0.2, or at least about 0.225. In some embodiments, the mole fraction ofbPL in the post-isolation β-propiolactone product stream can be about0.1-0.4, about 0.15-0.3, about 0.18-0.25, about 0.21-0.23, at leastabout 0.15, at least about 0.2, or at least about 0.22. Thepost-isolation β-propiolactone product stream can also include othercomponents including unreacted ethylene oxide (in mass fraction of about0.005-0.05, about 0.01-0.04, about 0.044, at most about 0.014, at mostabout 0.02, or at most about 0.05), unreacted carbon monoxide (in massfraction of about 0.0005-0.001, at most about 0.001, or at most about0.002), acetaldehyde (in mass fraction of about 0.0005-0.005, at mostabout 0.005, or at most about 0.01), succinic anhydride (in massfraction of about 0.0005-0.0051, at most about 0.005, or at most about0.01), carbonylation catalyst (in about 0-50 kg/hr, about 0.5-20 kg/hr,about 1-15 kg/hr, about 0-5 kg/hr, about 0.5-2 kg/hr, about 1-1.5 kg/hr,at most 1.4 kg/hr, at most about 2 kg/hr, at most 10 kg/hr, or at most20 kg/hr), and the remainder solvent. In some variations, thepost-isolation β-propiolactone product stream can includes carbonylationcatalyst components (in about 0-50 kg/hr, about 0.5-20 kg/hr, about 1-15kg/hr, about 0-5 kg/hr, about 0.5-2 kg/hr, about 1-1.5 kg/hr, at most1.4 kg/hr, at most about 2 kg/hr, at most 10 kg/hr, or at most 20kg/hr).

In some embodiments, the β-propiolactone product stream exiting thecarbonylation catalyst recycling system can have a temperature of about20-60° C., about 30-50° C., about 35-45° C., or about 40° C. In someembodiments, the β-propiolactone product stream exiting thecarbonylation catalyst recycling system can have a pressure of about1-15 bar, about 2-10 bar, or about 7 bar.

Carbonylation Catalyst Regeneration and Accumulation

The carbonylation catalyst may be recovered from the catalyst recyclingsystem in a form other than as active catalyst. Thus, with reference toFIG. 3, in some variations, retentate stream 324 may require furtherprocessing by one or more additional steps to regenerate thecarbonylation catalyst for use in the β-propiolactone productionsystem/production process.

Further, the carbonylation catalyst (or a component thereof) separatedfrom the β-propiolactone product stream may be accumulated through someinterval of time. The accumulated catalyst (or component) forms a spentcatalyst batch that is eventually reused (either in whole or in part) ina carbonylation process. The process for which the catalyst is re-usedmay or may not be the same process from which the catalyst was isolated.Likewise it may be reused for the same process but on another day or ina different reactor. This is in contrast to methods wherein theseparated catalyst is treated as a stream within the reaction processwhich is returned to the reactor within a relatively short period.

In certain embodiments where the carbonylation catalyst comprises acationic Lewis acid in combination with an anionic metal carbonyl, thecationic Lewis acid portion of the catalyst is captured from theβ-propiolactone product stream without the associated metal carbonyl. Incertain embodiments, the cationic Lewis acid is accumulated in a formwith a counterion other than the anionic metal carbonyl. In suchembodiments, the methods may include a further step of treating theaccumulated batch of cationic Lewis acid under conditions to swap anon-metal carbonyl anion associated with the accumulated Lewis acid witha metal carbonyl anion.

In certain embodiments where the carbonylation catalyst comprises acationic Lewis acid in combination with an anionic metal carbonyl, themetal carbonyl portion of the catalyst is captured from theβ-propiolactone product stream without the associated Lewis acid. Themetal carbonyl thus accumulated may be captured as an anionic metalcarbonyl (for example by anion exchange) or it may be accumulated inanother form such as a reduced metal species, a metal salt, a neutralmetal carbonyl, a mixed metal carbonyl complex, or some other form. Insuch embodiments, the methods may include a further step of treating theaccumulated species to regenerate a catalytically active metal carbonylcompound. In the case where an intact metal carbonyl anion isaccumulated (for example by capture on an anion exchange resin), suchsteps may include metathesis to free the metal carbonyl anion from theresin. This will typically entail flooding the resin with another anion(such as sodium chloride) to displace the metal carbonyl. The metalcarbonyl may then be obtained as its sodium salt and utilized to produceactive catalyst according to known catalyst synthesis procedures.Therefore, in certain embodiments, systems and methods described hereincomprise further steps of freeing accumulated metal carbonyl anion froma resin. In certain embodiments, such steps entail further steps ofutilizing accumulated metal carbonyl anion to regenerate active catalystby combining the accumulated metal carbonyl with a suitable Lewis acid.

In certain embodiments, the metal carbonyl may be accumulated in a formother than as an intact metal carbonyl anion. For example, inCO-deficient atmospheres, the metal carbonyl may lose one or more COligands to form multinuclear metal carbonyl species, salts, orprecipitate in elemental form. In other embodiments, a strong ligand maybe utilized to displace one or more CO ligands and aid in capture of themetal carbonyl as a new complex. It is known that such species can beutilized to regenerate well defined metal carbonyl compounds bytreatment under CO pressure. Therefore, in certain embodiments, systemsand methods described herein include further steps of regenerating thecatalytically active metal carbonyl species from a non-catalyticallyactive material accumulated from the β-propiolactone product stream. Incertain embodiments, such steps entail further steps of treatingaccumulated residue derived from a catalytically active metal carbonylcompound under conditions to regenerate a catalytically active metalcarbonyl suitable for reuse. In certain embodiments, such steps includea step of treating the accumulated residue under high CO pressure. Incertain embodiments, methods include the step of treating acobalt-containing residue accumulated from the β-propiolactone productstream under conditions of high CO pressure to convert it to dicobaltoctacarbonyl.

In certain embodiments where the accumulation of catalyst separated fromthe β-propiolactone product stream comprises steps of recovering two ormore separate catalyst components in separate recovered catalystbatches, additional steps of recombining recovered catalyst componentsmay be needed to produce active carbonylation catalyst. In some casesthe recovered catalyst components may be combined directly while inother steps one or more of the components may require processing asdescribed above prior to step of combining. In certain embodiments suchsteps entail a metathesis to recombine a recovered cationic Lewis acidwith a recovered metal carbonyl anion such as a carbonyl cobaltate.

The time interval required to accumulate a batch is dependent on themode of accumulation, and the scale and economics of any processesrequired to transform the accumulated catalyst residue into activecatalyst. In some embodiments, the time interval for accumulation of thecatalyst or residue is on the order of hours to days, but may be weeks.Therefore, in certain embodiments of any of the methods described above,the first time interval is in the range from about 1 hour to about 200hours. In certain embodiments, the first time interval is from about 2hours to about 8 hours, from about 4 hours to about 16 hours, from about12 hours to about 24 hours, or from about 16 hours to about 36 hours. Incertain embodiments, the first time interval is from about 1 day toabout 20 days, from about 1 day to about 3 days, from about 2 days toabout 5 days, from about 5 days to about 10 days, or from about 10 daysto about 20 days.

During this time, the carbonylation reactor may be fed from a reservoirof catalyst which is depleted as the amount of accumulated catalyst (orcatalyst residue) increases on the back end of the process. Additionaltime may be required to process the accumulated catalyst or catalystresidue to remanufacture active catalyst. Therefore, in some variations,some multiple of the first time interval have elapsed from the firsttime interval when the catalyst was accumulated to the later time atwhich the carbonylation reactor is fed with a catalyst feed streamcontaining catalyst derived from the catalyst accumulated during thefirst time interval. In certain embodiments the length of time betweenthe second time interval (during with catalyst recovered is fed toreactor), and the first time interval (during which the catalyst wasaccumulated) is on the order of about 1 to about 100 times the length ofthe first time interval. In other words, if the first time interval is10 hours, the second time interval would occur from about 10 hours toabout 2000 hours after the completion of the accumulation step. Incertain embodiments, the length of time between the second time intervaland the first time interval is from about 1 to about 10 times the lengthof the first time interval. In certain embodiments, the length of timebetween the second time interval and the first time interval is fromabout 1 to about 3 times, from about 2 to about 5 times, from about 4 toabout 10 times, from about 10 to about 50 times, from about 40 to about80 times, or from about 50 to about 100 times, the length of the firsttime interval. In certain embodiments, the length of time between thesecond time interval and the first time interval is greater than 100times the first time interval.

Continuous Replacement of Catalyst at Predetermined Rate

In certain variations, the carbonylation catalyst recycling system maybe configured to continuously or intermittently introduce to thecarbonylation reactor a catalyst replacement component that is differentfrom the carbonylation catalyst (e.g., from the carbonylation catalystsource) and may comprise a species selected from the group consisting ofthe Lewis acid, a precursor to the Lewis acid, the metal carbonyl, and aprecursor to the metal carbonyl.

In some embodiments, the catalyst replacement component comprises theLewis acid. In some embodiments, the catalyst replacement componentcomprises a precursor to the Lewis acid. In some embodiments, thecatalyst replacement component comprises the metal carbonyl. In someembodiments, the catalyst replacement component comprises a precursor tothe metal carbonyl.

In some embodiments, the catalyst replacement component is introduced ata rate that results in less than 10% variation in the rate of thecarbonylation reaction over a period of one hour. In some embodiments,the catalyst replacement component is introduced at a rate that resultsin less than 5% variation in the rate of the carbonylation reaction overa period of one hour.

In some embodiments, the rate at which the catalyst replacementcomponent is added to the carbonylation reactor is determined by therate at which the carbonylation reaction rate has been observed todecrease. In some embodiments, the rate at which the one or morecatalyst replacement components are added to the carbonylation reactoris directly proportional to the rate at which the carbonylation reactionrate has been observed to decrease.

In some embodiments, the one or more catalyst replacement components areintroduced continuously to the carbonylation reactor at the same ratethat the carbonylation reaction rate is observed to decrease. In someembodiments, the one or more catalyst replacement components areintroduced intermittently to the carbonylation reactor to produce anaverage rate which matches the rate at which the carbonylation reactionrate has been observed to decrease.

Thus, if the carbonylation reaction rate has been observed to decrease5% over the course of a time period, the catalyst replacement componentmay either be added continuously or intermittently at such a rate that5% of the initial amount of Lewis acid or metal carbonyl present in thecarbonylation reactor is added over that same time period. In someembodiments, the catalyst replacement component is added continuously.In some embodiments, the catalyst replacement component is added everyhour. In some embodiments, the catalyst replacement component is addedevery 30 minutes. In some embodiments, the catalyst replacementcomponent is added every 15 minutes. In some embodiments, the catalystreplacement component is added every 10 minutes. In some embodiments,the catalyst replacement component is added every 5 minutes. In someembodiments, the catalyst replacement component is added every minute.

One of skill in the art will appreciate that the shorter the intervalsat which the one or more catalyst replacement components are added, theless variation in the overall carbonylation reaction rate will beobserved. It should be recognized, however, that this must be balancedagainst other considerations such as the complexity of making multipleadditions.

Recycling to BPL Production System/Production Process

In some embodiments, the carbonylation catalyst and/or solvent streammay be recycled to the feed stream or to the carbonylation reactor. Insome embodiments, the portion of the solvent and/or catalyst from theβ-propiolactone product stream recycled to the carbonylation reactor orfeed stream ranges from about 0% to about 100%. In some embodiments, theportion of the solvent and/or catalyst from the β-propiolactone productstream recycled to the carbonylation reactor or feed stream is about100%, about 90%, about 80%, about 70%, about 60%, about 50%, about 40%,about 30%, about 20%, about 10%, or about 0%. In some embodiments, adifferent percentage of the catalyst, as compared to the solvent isrecycled, i.e., the proportions of either the catalyst or solventcomponent do not need to be equal.

BPL Purification System (and Solvent Recycle)

After the catalyst isolation system, the post-isolation carbonylationstream (i.e., post-isolation β-propiolactone product stream) can be fedto the BPL Purification system. The BPL purification system can separatebPL into a BPL purified stream from low-boiling impurities before itenters the polymerization reaction system, where high purity bPL can berequired. In some embodiments, the BPL purified stream can have at leastabout 90 wt % bPL, at least about 95 wt % bPL, at least about 98 wt %bPL, at least about 99 wt % bPL, at least about 99.3 wt % bPL, at leastabout 99.5 wt % bPL, at least about 99.8 wt %, or at least about 99.9 wt%. In some embodiments, the BPL purified stream can have at most about 1wt % solvent, at most about 0.5 wt % solvent, or at most about 0.1 wt %solvent. In some embodiments, the BPL purification system can alsocreate a solvent recycle stream. In some embodiments, the BPLpurification system can separate the bPL from the other components inthe post-isolation carbonylation stream such as solvent, unreactedethylene oxide, unreacted carbon monoxide, secondary reaction productacetaldehyde, secondary reaction product succinic anhydride, andcarbonylation catalyst or components thereof that was not isolated inthe catalyst isolation system. The separation of bPL from the othercomponents in the post-isolation carbonylation stream can beaccomplished by various methods known to those of ordinary skill in theart.

Carbonylation catalyst components may include, for example, compoundsproduced by degradation of the catalyst, compounds used to produce thecatalyst, metals or metal ions which were part of the catalyst, anyorganic compounds which were part of the catalyst, metal carbonyls ormetal complexes which were part of the catalyst. For example, in someembodiments, carbonylation catalyst components are carbonyl cobaltate,aluminum salen compounds, aluminum porphyrin compounds, aluminumsalophen compounds, cobalt or cobalt ions, or aluminum or aluminum ions,or any combinations thereof.

In some embodiments, the temperature in the BPL purification system canbe at most about 150° C., at most about 125° C., at most about 115° C.,at most about 105° C., or at most about 100° C. When bPL is exposed totemperatures greater than 100° C., the bPL can potentially decompose orbe partially polymerized. Accordingly, the bPL can be purified withoutbeing exposed to temperatures of about 150° C., 125° C., 115° C., 105°C., or 100° C.

In some embodiments, the separation is performed by exploiting theboiling point differential between the beta-propiolactone and the othercomponents of the carbonylation product stream, primarily the solvent.In some embodiments, the boiling point of the solvent is lower than theboiling point of the beta-propiolactone. In some embodiments, thesolvent is volatilized (e.g., evaporated) from the BPL purification feedalong with other lighter components (e.g., ethylene oxide &acetaldehyde), leaving behind bPL, other heavier compounds (e.g.,catalyst and succinic anhydride) and some leftover solvent from the BPLpurification feed. In some embodiments, this includes exposing the BPLpurification feed to reduced pressure. In some embodiments, thisincludes exposing BPL purification feed to increased temperature. Insome embodiments, this includes exposing the BPL purification feed toboth reduced pressure and increased temperature.

In some embodiments, the pressure is selected so that the boiling pointof the solvent is reduced by about 5° C. as compared to the boilingpoint at atmospheric pressure. In some embodiments, the pressure isselected so the boiling point of the solvent is reduced by about 10° C.as compared to the boiling point at atmospheric pressure. In someembodiments, the pressure is selected so the boiling point of thesolvent is reduced by about 20° C. as compared to the boiling point atatmospheric pressure. In some embodiments, the pressure is selected sothe boiling point of the solvent is reduced by about 50° C. as comparedto the boiling point at atmospheric pressure.

In some embodiments, the increased temperature is above the boilingpoint of the solvent but below the boiling point of thebeta-propiolactone, at the selected pressure. In some embodiments, thetemperature is at least about 20° C. below the boiling point of thebeta-propiolactone. In some embodiments, the temperature is at leastabout 30° C. below the boiling point of the beta-propiolactone. In someembodiments, the temperature is at least about 50° C. below the boilingpoint of the beta-propiolactone.

In some embodiments, the reduced pressure is in the range from about 1Torr to about 760 Torr. In some embodiments, the pressure is in therange of about 1 Torr to about 400 Torr. In some embodiments, thepressure is in the range of about 5 Torr to about 200 Torr. In someembodiments, the pressure is in the range of about 10 Torr to about 100Torr. In some embodiments, the pressure is in the range of about 20 Torrto about 50 Torr. In some embodiments, the pressure is about 50 Torr,about 100 Torr, about 150 Torr, about 200 Torr, about 250 Torr, about300 Torr, about 400 Torr about 500 Torr, about 600 Torr or about 700Torr.

In some embodiments, the separation step is performed at a pressurebelow about 100 Torr and at a temperature above about 120° C. In someembodiments, the separation step is performed at a pressure below about50 Torr and at a temperature above about 100° C. In some embodiments,the separation step is performed at a pressure below about 50 Torr andat a temperature above about 50° C. In some embodiments, the separationstep is performed at a pressure below about 50 Torr and at a temperatureabove about 110° C. In some embodiments, the separation step isperformed at a pressure below about 50 Torr and at a temperature aboveabout 90° C. In some embodiments, the separation step is performed at apressure below about 20 Torr and at a temperature above about 60° C. Insome embodiments, the separation step is performed at a pressure belowabout 10 Torr and at a temperature above about 50° C.

In some embodiments, the separation may be effected in a sequence ofsteps, each operating at an independent temperature and pressure. Forexample, in one embodiment, two steps may be used to obtain a moreeffective separation of beta-propiolactone, or a separate separationstep may be used to isolate certain reaction by-products. In someembodiments, when a mixture of solvents is used, multiple separationsteps may be required to remove particular solvents, individually or asa group, and effectively isolate the beta-propiolactone.

In certain embodiments, the separation of the beta-propiolactone fromthe BPL purification feed is performed in two stages. In someembodiments the process includes a preliminary separation step to removeone or more components of the BPL purification feed having boilingpoints below that of the beta-propiolactone product.

In some embodiments, the preliminary separation step includes separatingthe BPL purification feed into a gas stream comprising ethylene oxide,solvent, and bPL (and potentially carbon monoxide, acetaldehyde, and/orbPL); and a liquid stream comprising beta-propiolactone, carbonylationcatalyst (and potentially succinic anhydride and/or solvent). In thesecond step of separation, the liquid stream is further separated into abeta-propiolactone stream comprising beta-propiolactone, a solventstream comprising solvent, and potentially a catalyst and succinicanhydride purge stream. The gas stream can also be further separatedinto a solvent stream comprising solvent, a light gases streamcomprising solvent and ethylene oxide (and potentially acetaldehyde),and a liquid bPL stream comprising bPL and solvent. The liquid bPLstream can join with the liquid stream prior to separation of the liquidstream and form a combined feed to the second separation step. In someembodiments, the solvent stream from the second separation step and/orthe solvent stream from the gas stream separation can form the solventrecycle stream which can be fed to the carbonylation reaction system orto a solvent reservoir.

In some embodiments where one or more solvents with a boiling pointlower than that of the beta-propiolactone are present, the lower boilingsolvent may be volatilized (e.g., evaporated) from the BPL purificationfeed in a preliminary separation step, leaving behind a mixturecomprising catalyst, beta-propiolactone, other solvents (if any) andother compounds in the BPL purification stream which is then furthertreated to separate the beta-propiolactone stream.

In certain embodiments where the separation is performed in two stages,the first step of separation comprises exposing the reaction stream tomildly reduced pressure to produce the gas stream and the liquid stream.In certain embodiments where the separation is performed in two stages,the gas stream can be returned to the carbonylation step.

In certain embodiments, the separation of the beta-propiolactone fromthe BPL purification feed is performed in three stages. In the firststep of separation, the BPL purification feed is separated into agaseous stream comprising ethylene oxide, solvent, and bPL (andpotentially carbon monoxide and/or acetalhydride); and a liquid streamcomprising solvent, beta-propiolactone, and carbonylation catalyst (andpotentially succinic anhydride). In the second step of separation, thegaseous stream is separated into a solvent side stream comprisingsolvent; a light gas stream comprising ethylene oxide and solvent (andpotentially carbon monoxide and/or acetaldehyde); and second liquidstream comprising solvent and bPL. In the third step of separation, thesecond liquid stream and the first liquid stream are combined andseparated into a gaseous solvent stream comprising solvent, a purifiedBPL stream comprising bPL, and potentially a catalyst and succinicanhydride purge stream. In some embodiments, the solvent side streamand/or the gaseous solvent stream can be used as the solvent recyclestream for use in the carbonylation reaction system or can be stored ina solvent storage tank.

In certain embodiments where the separation is performed in threestages, the first step of separation comprises exposing the BPLpurification feed to atmospheric pressure. In certain embodiments wherethe separation is performed in three stages, the second step ofseparation comprises exposing the gaseous stream to atmosphericpressure. In certain embodiments where the separation is performed inthree stages, the third step of separation comprises exposing thegaseous stream to a vacuum or reduced pressure. In certain embodiments,the reduced pressure is between about 0.05-0.25 bara. In certainembodiments, the reduced pressure is between about 0.1-0.2 bara or about0.15 bara.

In certain embodiments, the separation of the beta-propiolactone fromthe BPL purification feed is performed in four stages. In the first stepof separation, the BPL purification feed is separated into a gaseousstream comprising ethylene oxide, solvent, and bPL (and potentiallycarbon monoxide and/or acetalhydride); and a liquid stream comprisingsolvent, beta-propiolactone, and carbonylation catalyst (and potentiallysuccinic anhydride). In the second step of separation, the gaseousstream is separated into a solvent side stream comprising solvent; alight gas stream comprising ethylene oxide and solvent (and potentiallycarbon monoxide and/or acetaldehyde); and second liquid streamcomprising solvent and bPL. In the third step of separation, the secondliquid stream and the first liquid stream are combined and separatedinto a gaseous solvent stream comprising solvent, a purified BPL streamcomprising bPL, and potentially a catalyst and succinic anhydride purgestream. In the fourth step of separation, the light gas stream isseparated into a third solvent stream comprising solvent and a secondlight gas stream comprising ethylene oxide (and potentially carbonmonoxide and/or acetaldehyde). In some embodiments, the solvent sidestream, the gaseous solvent stream, and/or the third solvent stream canbe used as the solvent recycle stream for use in the carbonylationreaction system or can be stored in a solvent storage tank.

In certain embodiments where the separation is performed in four stages,the first step of separation comprises exposing the BPL purificationfeed to atmospheric pressure. In certain embodiments where theseparation is performed in four stages, the second step of separationcomprises exposing the gaseous stream to atmospheric pressure. Incertain embodiments where the separation is performed in four stages,the third step of separation comprises exposing the combined liquidstream to a vacuum or reduced pressure. In certain embodiments, thereduced pressure is between about 0.05-0.25 bara. In certainembodiments, the reduced pressure is between about 0.1-0.2 bara or about0.15 bara. In certain embodiments where the separation is performed infour stages, the fourth step of separation comprises exposing the lightgas stream to atmospheric pressure.

In some embodiments, the BPL purification system can include at leastone distillation column to separate bPL from the other components in thepost-isolation carbonylation stream. In some embodiments, the BPLpurification system includes at least two distillation columns. In someembodiments, the BPL purification system includes at least threedistillation columns. In some embodiments, at least one of thedistillation columns is a stripping column (i.e., stripper). In someembodiments, at least one of the distillation columns is a vacuumcolumn. In some embodiments, the BPL purification system can include aninitial evaporator, wherein the post-isolation carbonylation stream isfirst fed to an evaporator in the BPL purification system. Theevaporator can perform a simple separation between the solvent and thebPL in the post-isolation carbonylation stream. The evaporator canreduce loads on subsequent distillation columns making them smaller. Insome embodiments, the evaporator can reduce loads on subsequentdistillation columns making them smaller by evaporating solvent in thepost-isolation carbonylation stream at about atmospheric pressure andabout 100° C.

FIG. 16 illustrates an exemplary embodiment of the BPL Purificationsystem disclosed herein.

Feed Stream

As depicted in FIG. 16, in some embodiments of the exemplary system,feed 1616 to BPL purification system 1617 can be the post-isolationcarbonylation product stream (i.e., post-isolation β-propiolactoneproduct stream). In other embodiments, the feed to the BPL purificationsystem can be the carbonylation product stream. In some embodiments, thefeed to BPL purification system is at least about 10000 kg/hr, at leastabout 11000 kg/hr, at least about 12000 kg/hr, at least about 13000kg/hr, at least about 13777 kg/hr, at least about 20000 kg/hr, at leastabout 50000 kg/hr, at least about 100000 kg/hr, at least about 110000kg/hr, at least about 120000 kg/hr, at least about 130000 kg/hr, or atleast about 137770 kg/hr. In some embodiments, the feed to BPLpurification system is about 10000 kg/hr, about 11000 kg/hr, about 12000kg/hr, about 13000 kg/hr, about 13777 kg/hr, about 20000 kg/hr, about50000 kg/hr, about 100000 kg/hr, about 110000 kg/hr, about 120000 kg/hr,about 130000 kg/hr, or about 137770 kg/hr. In some embodiments, the feedto BPL purification system is between about 10000 kg/hr and about 13777kg/hr, between about 11000 kg/hr and about 13777 kg/hr, between about12000 kg/hr and about 13777 kg/hr, between about 13000 kg/hr and about13777 kg/hr, between about 10000 kg/hr and 137770 kg/hr, between about11000 kg/hr and about 137770 kg/hr, between about 12000 kg/hr and about137770 kg/hr, between about 13000 kg/hr and about 137770 kg/hr, betweenabout 13777 kg/hr and about 137770 kg/hr, between about 20000 kg/hr andabout 137770 kg/hr, between about 50000 kg/hr and about 137770 kg/hr,between about 100000 kg/hr and about 137770 kg/hr, between about 110000kg/hr and about 137770 kg/hr, between about 120000 kg/hr and about137770 kg/hr, or between about 130000 kg/hr and about 137770 kg/hr. Insome embodiments, the feed to BPL purification system has a bPL wt %between about 10-30, about 15-28, about 18-25, about 20-25, about 22-23,about 22.5, or at least 22.5. In some embodiments, the feed to BPLpurification system has solvent (e.g., THF) wt % between 60-90, about65-85, about 70-80, about 72-78, about 74-76, about 75, about 75.8, orat least about 75. In some embodiments, the feed to BPL purificationsystem has a CO wt % between about 0-0.2, about 0.05-0.15, about 0.1, orat most about 0.2. In some embodiments, the feed to BPL purificationsystem has an acetaldehyde wt. % between about 0-0.2, about 0.05-0.15,about 0.1, at most about 0.1, or at most about 0.2. In some embodiments,the feed to BPL purification system has a succinic anhydride wt. %between about 0-0.2, about 0.05-0.15, about 0.1, at most about 0.1, orat most about 0.2. In some embodiments, the feed to BPL purificationsystem has an EO wt % between about 0-3, about 0.5-2, about 1-2, about1.4, at most about 1.4, or at most about 2. In some embodiments, thefeed to the BPL purification system has trace amounts of carbonylationcatalyst. In some embodiments, the feed to the BPL purification systemhas trace amounts of carbonylation catalyst components.

Evaporator

In some embodiments, the feed to the BPL purification system can be fedto evaporator 1628. In some embodiments, the evaporator can operate atmost about 5 bara, at most about 4 bara, at most about 3 bara, at mostabout 2 bara, at most about atmospheric pressure (i.e., 1 bara), or atabout atmospheric pressure. In some embodiments, the evaporator canoperate at a temperature between about 80-120° C., between about 90-100°C., between about 95-105° C., at about 100° C., at most about 100° C.,at most about 105° C., at most about 110° C., or at most about 120° C.In some embodiments, the evaporator is a flash tank. Referring again toFIG. 16, in the exemplary system evaporator 1628 can separate the feedinto overhead stream 1629 and bottoms stream 1630. Overhead stream 1629can comprise mainly of THF with low boiling point components (e.g., CO,EO, acetaldehyde) and a small amount of bPL. In some embodiments,overhead stream 1629 can have a mass flow rate of at least about 9000kg/hr, at least about 10000 kg/hr, at least about 11000 kg/hr, at leastabout 11500 kg/hr, or at least about 12000 kg/hr. In some embodiments,overhead stream 1629 can have a solvent (e.g., THF) wt % of about 75-95,about 80-90, about 85, about 86.7, at least about 75, at least about 80,at least about 85, or at least about 90. In some embodiments, overheadstream 1629 can have a bPL wt % of about 0-20, about 5-20, about 8-15,about 10, about 11.5, at most about 25, at most about 20, at most about15, at most about 11.5, at most about 10, or at most about 5. In someembodiments, overhead stream 1629 can have a carbon monoxide wt % ofabout 0-0.2, about 0.05-0.15, about 0.1, at most about 0.2, or at mostabout 0.1. In some embodiments, overhead stream 1629 can have anethylene oxide wt % of about 0-5, about 0.5-3, about 1-2, about 1.6, atmost 5, at most 3, at most 2, at most 1.6. In some embodiments, overheadstream 1629 can have an acetaldehyde wt % of about 0-0.4, about 0.1-0.3,about 0.2, at most about 0.4, or at most about 0.2.

In some embodiments, bottoms stream 1630 can have a mass flow rate of atleast about 500 kg/hr, at least about 1000 kg/hr, at least about 1500kg/hr, at least about 2000 kg/hr, at least about 2200 kg/hr, at leastabout 3000 kg/hr, at least about 4000 kg/hr, at least about 5000 kg/hr,at least about 10000 kg/hr, at least about 15000 kg/hr, at least about20000 kg/hr, at least about 22000 kg/hr, at least about 30000 kg/hr. Insome embodiments, bottoms stream 1630 can have a mass flow rate ofbetween about 500 kg/hr and about 3000 kg/hr, between about 1000 kg/hrand about 3000 kg/hr, between about 1500 kg/hr and about 3000 kg/hr,between about 2000 kg/hr and about 3000 kg/hr, between about 2200 kg/hrand about 3000 kg/hr, between about 500 kg/hr and about 30000 kg/hr,between about 1000 kg/hr and about 30000 kg/hr, between about 1500 kg/hrand about 30000 kg/hr, between about 2000 kg/hr and about 30000 kg/hr,between about 2200 kg/hr and about 30000 kg/hr, between about 3000 kg/hrand about 30000 kg/hr, between about 4000 kg/hr and about 30000 kg/hr,between about 5000 kg/hr and about 30000 kg/hr, between about 10000kg/hr and about 30000 kg/hr, between about 15000 kg/hr and about 30000kg/hr, between about 20000 kg/hr and about 30000 kg/hr, between about22000 kg/hr and about 30000 kg/hr. In some embodiments, bottoms stream1630 can have a bPL wt % of about 60-95, about 65-90, about 70-85, about75-85, about 79.7, about 80, at least about 65, at least about 70, atleast about 75, at least about 79.7, at least about 85. In someembodiments, bottoms stream 1630 can have a solvent wt % of about 5-40,about 10-30, about 15-25, about 18-20, about 19.2, about 20, at most 40,at most 30, at most 25, at most 20, at most 19.2, at most 15, or at most10. In some embodiments, bottoms stream 1630 can have an ethylene oxidewt % of about 0-0.4, about 0.1-0.3, about 0.2, at most about 0.4, or atmost about 0.2. In some embodiments, bottoms stream 1630 can have asuccinic anhydride wt % of about 0-2, about 0.2-1.6, about 0.4-1.2,about 0.6-1, about 0.7-0.9, at most about 2, at most about 1, at mostabout 0.8. In some embodiments, the bottoms stream 1630 can have acarbonylation catalyst wt % of about 0-0.2, about 0.05-0.15, about 0.1,at most about 0.2, or at most about 0.1. In some embodiments, thebottoms stream 1630 can have a carbonylation catalyst component wt % ofabout 0-0.2, about 0.05-0.15, about 0.1, at most about 0.2, or at mostabout 0.1.

Solvent Purification Column

Referring again to FIG. 16, in the exemplary system depicted overheadstream 1629 can be sent to solvent purification column 1631. The solventpurification column can be a distillation column. In some embodiments,the solvent purification column can be a stripping column or stripper.In some embodiments, the solvent purification column can operate at mostabout 5 bara, at most about 4 bara, at most about 3 bara, at most about2 bara, at most about atmospheric pressure (i.e., 1 bara), or at aboutatmospheric pressure. In some embodiments, the evaporator can operate ata temperature of at most about 100° C., at most about 105° C., at mostabout 110° C., or at most about 120° C. In some embodiments, an overheadtemperature is maintained at about 20-60° C., about 30-50° C., about40-50° C., about 44° C. In some embodiments, the solvent purificationcolumn can prevent bPL from getting into any vent streams. In someembodiments, solvent purification column can have at least 12 stageswith a condenser as stage 1. In some embodiments, solvent purificationcolumn can have an internal cooler which can create a side stream. Insome embodiments, solvent purification column can have an internalcooler above the side stream withdrawal. In some embodiments, internalcooler can be between stages in the middle of the column. In someembodiments, internal cooler can be between stages 5 and 6 of thesolvent purification column. In some embodiments, solvent purificationcolumn can separate overhead stream 1629 into overhead stream 1632,bottoms stream 1634, and side stream 1633. Overhead stream 1632 cancomprise low boiling components (e.g., EO, CO, acetaldehyde) and aroundhalf solvent. Bottoms stream 1634 can comprise mainly bPL and solvent.In some embodiments, solvent purification column can recover at least 90wt %, at least 95 wt %, at least 98 wt %, at least 99 wt %, or at least99.5 wt % of bPL from overhead stream 1629 in bottoms stream 1634.

In some embodiments, overhead stream 1632 can have a mass flowrate of atleast 200 kg/hr, at least 300 kg/hr, at least 400 kg/hr, at least 411kg/hr, at least 500 kg/hr, at least 1000 kg/hr, at least 1500 kg/hr, atleast 2000 kg/hr, at least 3000 kg/hr, at least 4000 kg/hr, at least4110 kg/hr, or at least 5000 kg/hr. In some embodiments, overhead stream1632 can have a mass flowrate of between 200 kg/hr and 500 kg/hr,between 300 kg/hr and 500 kg/hr, between 400 kg/hr and 500 kg/hr,between 411 kg/hr and 500 kgr/hr, between 200 kg/hr and 5000 kg/hr,between 300 kg/hr and 5000 kg/hr, between 400 kg/hr and 5000 kg/hr,between 411 kg/hr and 5000 kgr/hr. In some embodiments, overhead stream1632 can have a solvent (e.g., THF) wt % of about 30-70, about 40-60,about 45-55, about 50-55, about 50, about 53.9, at most 75, at most 65,at most 60, at most 55, at most 53.9, at most 50, at most 45. In someembodiments, overhead stream 1632 can have an ethylene oxide wt % ofabout 20-60, about 30-50, about 35-45, about 37-43, about 40.6, at leastabout 20, at least about 25, at least about 30, at least about 35, atleast about 40, at least about 40.6, at least about 45, or at leastabout 50. In some embodiments, overhead stream 1632 can have a carbonmonoxide wt % of about 0-5, about 0.5-3, about 1-2, about 1.5-2, about1.7, at most about 5, at most about 3, at most about 2, at most about1.7, at most about 1. In some embodiments, overhead stream 1632 can havea acetaldehyde wt % of about 0-10, about 1-7, about 2-5, about 3-4.5,about 3.5-4, about 3.8, at most about 10, at most about 7, at most about5, at most about 4, at most about 3.8, at most about 3.

In some embodiments, bottoms stream 1634 can have a mass flowrate of atleast about 1000 kg/hr, at least about 1200 kg/hr, at least about 1400kg/hr, at least about 1600 kg/hr, at least about 1643 kg/hr, at leastabout 1800 kg/hr, at least about 4000 kg/hr, at least about 7500 kg/hr,at least about 10000 kg/hr, at least about 12000 kg/hr, at least about14000 kg/hr, at least about 16000 kg/hr, at least about 16430 kg/hr, orat least about 18000 kg/hr. In some embodiments, bottoms stream 1634 canhave a mass flowrate of about 1000 kg/hr, about 1200 kg/hr, about 1400kg/hr, about 1600 kg/hr, about 1643 kg/hr, about 1800 kg/hr, about 4000kg/hr, about 7500 kg/hr, about 10000 kg/hr, about 12000 kg/hr, about14000 kg/hr, about 16000 kg/hr, about 16430 kg/hr, or about 18000 kg/hr.In some embodiments, bottoms stream 1634 can have a mass flowrate ofbetween 1000 kg/hr and 1800 kg/hr, between 1200 kg/hr and 1800 kg/hr,between 1400 kg/hr and 1800 kg/hr, between 1600 kg/hr and 1800 kg/hr,between 1643 kg/hr and 1800 kg/hr, between 1000 kg/hr and 18000 kg/hr,between 1200 kg/hr and 18000 kg/hr, between 14000 kg/hr and 18000 kg/hr,between 16000 kg/hr and 18000 kg/hr, between 1643 kg/hr and 18000 kg/hr,between 4000 kg/hr and 18000 kg/hr, between 10000 kg/hr and 18000 kg/hr,or between 16000 kg/hr and 18000 kg/hr. In some embodiments, bottomsstream 1634 can have a bPL wt % of about 60-95, about 70-90, about75-85, about 80, about 80.4, at least 60, at least 70, at least 75, atleast 80, at least 80.4, at least 85, at least 90, or at least 95. Insome embodiments, bottoms stream 1634 can have a solvent wt % of about5-40, about 10-30, about 15-25, about 20, about 19.5, at most 40, atmost 30, at most 25, at most 20, at most 19.5, at most 15, or at most10. In some embodiments, bottoms stream 1634 can have an ethylene oxidewt % of about 0-0.4, about 0.1-0.3, about 0.2, at most about 0.4, or atmost about 0.2.

In some embodiments, side stream 1633 can have a mass flow rate of atleast about 6000 kg/hr, at least about 7000 kg/hr, at least about 8000kg/hr, at least about 9000 kg/hr, at least about 9500 kg/hr, at leastabout 9508 kg/hr, at least about 10000 kg/hr, at least about 20000kg/hr, at least about 40000 kg/hr, at least about 60000 kg/hr, at leastabout 70000 kg/hr, at least about 80000 kg/hr, at least about 90000kg/hr, at least about 95000 kg/hr, at least about 95080 kg/hr, or atleast about 100000 kg/hr. In some embodiments, side stream 1633 can havea mass flow rate of about 6000 kg/hr, about 7000 kg/hr, about 8000kg/hr, about 9000 kg/hr, about 9500 kg/hr, about 9508 kg/hr, about 10000kg/hr, about 20000 kg/hr, about 40000 kg/hr, about 60000 kg/hr, about70000 kg/hr, about 80000 kg/hr, about 90000 kg/hr, about 95000 kg/hr,about 95080 kg/hr, or about 100000 kg/hr. In some embodiments, sidestream 1633 can have a mass flow rate of between 6000 kg/hr and 10000kg/hr, between 7000 kg/hr and 10000 kg/hr, between 8000 kg/hr and 10000kg/hr, between 9000 kg/hr and 10000 kg/hr, between 9500 kg/hr and 10000kg/hr, between 9508 kg/hr and 10000 kg/hr, between 6000 kg/hr and 100000kg/hr, between 10000 kg/hr and 100000 kg/hr, between 20000 kg/hr and100000 kg/hr, between 40000 kg/hr and 100000 kg/hr, between 60000 kg/hrand 100000 kg/hr, between 70000 kg/hr and 100000 kg/hr, between 80000kg/hr and 100000 kg/hr, or between 90000 kg/hr and 100000 kg/hr,between. In some embodiments, side stream 1633 can have a solvent wt %of at least 95, at least 98, at least 99, at least 99.7. In someembodiments, side stream 1633 can have an ethylene oxide wt. % of about0-0.4, about 0.1-0.3, about 0.2, at most about 0.4, or at most about0.2. In some embodiments, side stream 1633 can have a bPL wt % of about0-0.2, about 0.05-0.15, about 0.1, at most about 0.1, or at most about0.2.

BPL Purification Column

Bottoms stream 1630 and bottoms stream 1634 can be combined and sent toBPL purification column 1635. BPL purification column can be adistillation column. In some embodiments, BPL purification column can bea vacuum column or a column operating under reduced pressure. In someembodiments, the operating pressure of the BPL purification column canbe less than atmospheric pressure (1 bara), less than about 0.5 bara,less than about 0.25 bara less than 0.2 bara, less than 0.15 bara, orabout 0.15 bara. In some embodiments, the BPL purification column caninclude a reboiler that can be maintained at most about 120° C., at mostabout 110° C., at most about 100° C., or about 100° C. In someembodiments, an overhead temperature is maintained at about 5-30° C.,about 10-20° C., about 12-16° C., about 14° C.

In some embodiments, BPL purification column can separate the combinedbottoms streams 1630 and 1634 into overhead stream 1636 and bottomsstream 1618 (i.e., BPL purified stream 1618). Bottoms stream 1618 can besubstantially pure bPL with minimal solvent. In some embodiments,bottoms stream 1618 can also include some heavy components such asresidual carbonylation catalyst and succinic anhydride. Thecarbonylation catalyst can be considered to be non-volatile and canaccumulate in the BPL purification column's sump. Accumulated catalystcan be removed periodically by purging sump when the catalyst wt %reaches a predefined value (e.g., at least 1 wt %, 2 wt %, 3 wt %, 4 wt%, or 5 wt %). In contrast to the carbonylation catalyst, succinicanhydride can have some volatility and if accumulated in the sump canproduce an undesirable rise in boiling temperature in the reboiler. Insome embodiments, succinic anhydride can also accumulate in the sump andcan be purged in the same manner the accumulated catalyst can be purged.In some embodiments, overhead stream 1636 can have a mass flow rate ofabout at least about 500 kg/hr, at least about 600 kg/hr, at least about700 kg/hr, at least about 750 kg/hr at least about 800 kg/hr, or atleast about 850 kg/hr. In some embodiments, overhead stream 1636 canhave a solvent wt % of at least about 95, at least about 98, at leastabout 99, at least about 99.1, or at least about 99.5. In someembodiments, overhead stream 1636 can have an ethylene oxide wt % ofabout 0-3, about 0.2-2, about 0.2-1.5, about 0.5-1, about 0.8, at mostabout 3, at most about 2, at most about 1, at most about 0.8, at mostabout 0.5. In some embodiments, overhead stream 1638 can have anacetaldehyde wt % of about 0-0.2, about 0.05-0.15, about 0.1, at mostabout 0.1, or at most about 0.2.

In some embodiments, bottoms stream 1618 can have a mass flow rate of atleast about 1000 kg/hr, at least about 2000 kg/hr, at least about 2500kg/hr, at least about 3000 kg/hr, at least about 3100 kg/hr, at leastabout 3500 kg/hr, at least about 4000 kg/hr, at least about 5000 kg/hr,at least about 1000 kg/hr, at least about 20000 kg/hr, at least about35000 kg/hr, at least about 36380 kg/hr, or at least about 40000 kg/hr.In some embodiments, bottoms stream 1618 can have a mass flow rate ofabout 2000 kg/hr, about 2500 kg/hr, about 3000 kg/hr, about 3500 kg/hr,about 3638 kg/hr, about 4000 kg/hr, about 5000 kg/hr, about 1000 kg/hr,about 20000 kg/hr, about 35000 kg/hr, about 36380 kg/hr, or about 40000kg/hr. In some embodiments, bottoms stream 1618 can have a mass flowrate of between 1000 kg/hr and 4000 kg/hr, or between 1000 kg/hr and40000 kg/hr. In some embodiments, bottoms stream 1618 can have a bPL wt% of at least about 95, at least about 98, at least about 99, at leastabout 99.3, or at least about 99.5. In some embodiments, bottoms stream1618 can have a solvent wt. % of about 0-0.2, about 0.05-0.15, about0.1, at most about 0.1, or at most about 0.2. In some embodiments,bottoms stream 1618 can have a succinic anhydride wt % of about 0-3,about 0.1-2, about 0.2-1, about 0.5-1, about 0.6, at most about 3, atmost about 2, at most about 1, at most about 0.6, at most about 0.5. Insome embodiments, bottoms stream 1618 can have trace amounts ofcarbonylation catalyst. In some embodiments, BPL purification column canhave a purge for the carbonylation catalyst and/or succinic anhydride inthe bottoms stream 1618. In some embodiments, the purge can be a valve.

Light Gas Column

Overhead stream 1632 can be sent to light gas column 1637 to beseparated into overhead stream 1639 and bottoms stream 1638. The lightgas column can be a distillation column. In some embodiments, the lightgas column can operate at most about 5 bara, at most about 4 bara, atmost about 3 bara, at most about 2 bara, at most about atmosphericpressure (i.e., 1 bara), or at about atmospheric pressure. In someembodiments, light gas column can include a partial condenser. In someembodiments, the partial condenser operates at a temperature of at about0-20° C., about 5-15° C., about 10-15° C., about 10-13° C. In someembodiments, the temperature maintained at the bottom of light gascolumn is about 20-70° C., about 40-60° C., about 45-55° C., or about50° C. In some embodiments, the overhead temperature maintained in lightgas column can be about −10-10° C., about −5-5° C., about −2-3° C., orabout 1° C. Overhead stream 1639 can comprise mostly of the acetaldehydeproduced in the carbonylation reaction system as well as low boilingpoint ethylene oxide. In some embodiments, overhead stream 1639 can bedisposed of (e.g., incinerator, flare, etc.) so acetaldehyde does notaccumulate in the overall production system/production process.

In some embodiments, overhead stream 1639 can have a mass flow rate ofabout 50 kg/hr, about 100 kg/hr, about 150 kg/hr, about 175 kg/hr, about200 kg/hr, about 250 kg/hr, at least 500 kg/hr, at least 1000 kg/hr, atleast 1500 kg/hr, at least 2000 kg/hr, or at least 2500 kg/hr. In someembodiments, overhead stream 1639 can have a mass flow rate of between50 kg/hr and 250 kg/hr, between 100 kg/hr and 250 kg/hr, between 200kg/hr and 250 kg/hr, or between 50 kg/hr and 2000 kg/hr. In someembodiments, overhead stream 1639 can have an ethylene oxide wt % of atleast about 70, at least about 75, at least about 80, at least about 85,at least about 89.5, at least about 90, or at least about 95. In someembodiments, overhead stream 1639 can have an acetaldehyde wt % of about0-15, about 1-10, about 2-8, about 6.1, at most about 15, at most about10, at most about 6.1, at most about 5, or at most about 2. In someembodiments, overhead stream 1639 can have a carbon monoxide wt % ofabout 0-12, about 1-10, about 2-6, about 4.10, at most about 12, at mostabout 10, at most about 6, at most about 5, at most about 4.1, or atmost about 2. In some embodiments, overhead stream 1639 can have asolvent wt. % of about 0-2, about 0.1-1, about 0.2-0.6, about 0.4, atmost about 2, at most about 1, at most about 0.5, at most about 0.4, orat most about 0.2.

In some embodiments, bottoms stream 1638 can have a mass flow rate ofabout 50 kg/hr, about 150 kg/hr, about 200 kg/hr, about 235 kg/hr, about250 kg/hr, about 300 kg/hr or about 350 kg/hr. In some embodiments,bottoms stream 1638 has a solvent wt % of at least about 75, at leastabout 80, at least about 85, at least about 90, at least about 93.9, atleast about 95, at least about 98, or at least about 99. In someembodiments, bottoms stream 1638 has an ethylene oxide wt % of about0-12, about 1-10, about 2-6, about 4, at most about 12, at most about10, at most about 8, at most about 5, at most about 4, or at most about2. In some embodiments, bottoms stream 1638 has an acetaldehyde wt % ofabout 0-10, about 0.5-5, about 1-4, about 1-3, about 2.2, at most about10, at most about 5, at most about 2.2, at most about 2, at most about1.

Solvent Recycle Stream

In some embodiments, side stream 1633, bottoms stream 1638, overheadstream 1636 or combinations thereof can form solvent recycle stream1623. In some embodiments, side stream 1633, bottoms stream 1638, andoverhead stream 1636 can be combined to form solvent recycle stream1623. In some embodiment, side stream 1633, bottoms stream 1638, and/oroverhead stream 1636 can be sent to a solvent recycle tank or storage.In some embodiments, the solvent recycle stream is fed back to thecarbonylation reaction system. In some embodiments, the solvent recyclestream fed to the carbonylation reaction system is from the solventrecycle tank or storage. In some embodiments, the solvent streamsentering and/or exiting the solvent recycle tank or storage can bepurified for example by passing the stream through an absorber to removepotential oxygen and/or moisture from the stream. In some embodiments,the solvent recycle tank or storage can be equipped with sensors todetermine the water and/or oxygen content in the storage tank.

Preferred Distillation System

In preferred embodiment, distillation sub-system consists of 3distillation columns: (1) Lights Removal column, (2) THF SolventRecovery column, and (3) bPL Purification column.

1. Lights Removal Column

The purpose of this column is to recover Ethylene Oxide (EO) for recycleback to the Carbonylation Reactor as well as to separate low-boilingimpurities such as Acetaldehyde (ACH). Distillate stream from thiscolumn may contain THF, EO, ACH or only EO and ACH. This column receivesa permeate stream from a carbonylation catalyst recovery zone and in ahighly preferred form has the following component with representativecompositions of THF (about 75.2 wt %), bPL (about 20.5 wt %), EthyleneOxide (about 4.1 wt %), Acetaldehyde (about 0.07 wt %), SuccinicAnhydride (about 0.02 wt %), traces of low and high boiling impurities,and trace residual carbonylation catalyst is fed to Lights Removaldistillation column. The distillation column is operated at the pressureof about 1.3 bara (column is operated at atmospheric pressure orslightly above atmospheric pressure). The reboiler temperature ismaintained at or below 105° C. Lights column distillate streamconsisting essentially of THF (about 93.4 wt %), EO (about 6.5 wt %),ACH (0.1 wt %), and traces of low boiling impurities is fed back to thecarbonylation reactor or to optional ACH removal system. The lightscolumn in a highly preferred form produces a bottoms stream consistingessentially of bPL (about 54.9 wt %), THF (about 45.0 wt %), SuccinicAnhydride (about 0.05 wt %), trace amounts of low- and high-boilingimpurities, and trace residual carbonylation catalyst and high-boilingimpurities is fed forward to THF Solvent Recovery column (2).

In some embodiments Lights Removal column can be operated in such a waythat Distillate stream consists of only Ethylene Oxide and Acetaldehydeand all THF is exiting the column with the Bottoms stream. If the lightsremoval column is operated in this configuration the distillate consistsessentially of EO (about 98.8 wt %), ACH (about 1.2 wt %), and trace oflow boiling impurities. The bottoms stream in this column configurationconsists essentially of THF (about 78.5 wt %), bPL (about 21.5 wt %),SAH (about 0.02 wt %), trace amounts of residual carbonylation catalyst,trace amounts of low- and high-boiling impurities.

Accumulation of Acetaldehyde within carbonylation/distillation systemcan be avoided by implementing a small purge from distillate stream orremoved from the distillate stream using an absorbent such as molecularsieves (non-limiting examples are Molecular Sieve 3A, 4A, 5A, 13X,etc.). Optionally, ACH is separated from EO using distillation orextractive distillation.

2. THF Solvent Recovery Column

The purpose of this column is to recover THF solvent for recycle back tothe carbonylation reactor. Due to the high boiling point of bPL (162° C.at atmospheric pressure) this column is operated at pressures belowatmospheric to limit the reboiler temperature below 105° C. and avoidautopolymerization of bPL. Distillate stream from this column containsessentially pure THF and bottoms stream of this column contains bPL,SAH, residual carbonylation catalyst, and trace amounts of high boilingimpurities.

Lights Column Bottom stream containing THF, bPL, SAH, residualcarbonylation catalyst, and trace amounts of low and high boilingimpurities is fed to THF Solvent Recovery distillation column (thecomposition of this stream is presented in the section above).Optionally, the THF solvent make-up stream may be fed to thiscolumn—this allows removal of O2, H2O, and BHT inhibitor from make-upTHF.

The distillation column is operated at the absolute pressure of about100 Torrs (column is operated under vacuum) and the reboiler temperatureis maintained at or below 105° C. The column is designed to minimize airintrusion into the column simplifying removal of O2 and H2O contaminantsfrom recycled THF Solvent stream in downstream unit operation.

The distillate stream from this column consisting of essentially pureTHF (purity greater than 99.9 wt %) with trace amounts of low- andhigh-boiling impurities is recycled back to the carbonylation reactor.Optionally and before it is recycled, this stream may be passed throughpurification system for removal of contaminants such as O2 and H2O.These impurities can be removed by any means known in the art such asabsorption, adsorption, extractive distillation, azeotropicdistillation, etc.

The bottoms stream consists of bPL (about 99.8 wt %), SAH (about 0.1 wt%), small amounts of residual carbonylation catalyst, and traces of low-and high-boiling impurities. This stream is fed forward to bPLPurification column.

3. bPL Purification Column

The purpose of this column is to recover purified bPL for subsequentproduction of PPL (poly-propiolactone). Due to high boiling point of bPL(162° C. at atmospheric pressure) this column is operated at pressuresbelow atmospheric to limit the reboiler temperature below 105° C. andavoid autopolymerization of bPL. The distillate stream from this columncontains essentially pure bPL. The bottoms stream of this columncontains residual bPL, SAH, residual carbonylation catalyst, and traceamounts of high boiling impurities. The Purified bPL stream is fedforward to Polymerization Reactor and bottoms stream is sent fordisposal or recovery of residual bPL and SAH. The bottoms stream fromTHF recovery column containing bPL (about 99.8 wt %), SAH (about 0.1 wt%), residual carbonylation catalyst, and traces of low- and high-boilingimpurities is fed to bPL Purification column.

The bPL purification column is in preferred form operated at theabsolute pressure of about 60 Torrs (column is operated under vacuum)and the reboiler temperature is maintained at or below 105° C. Thedistillate stream consisting of essentially pure bPL (purity greaterthan 99.9 wt %) with trace amounts of low- and high-boiling impuritiesis fed forward to bPL Polymerization reactor.

The Bottoms stream of this column consists of bPL (about 88.9 wt %), SAH(about 9.7 wt %), carbonylation catalyst (about 1.4 wt %), and tracehigh-boiling impurities. The amount of bPL in this bottoms stream isselected to avoid crystallization of SAH at the temperatures below itsmelting point of 119° C. and to limit the reboiler temperature to below105° C.

Polypropiolactone Production System/Production Process

With reference to FIG. 2, the relationship of the polypropiolactoneproduction system/production process with other unit operations, such asthe β-propiolactone purification system, the ion removal unit, and theglacial acrylic acid production system/production process, is depicted.

β-Propiolactone purification system 202 is configured to feed aβ-propiolactone product stream into polypropiolactone productionsystem/production process 210. Homogeneous catalyst delivery system 204is configured to feed a homogeneous polymerization catalyst into thepolymerization reactor of polypropiolactone production system/productionprocess 210. Polypropiolactone production system/production process 210is configured to polymerize β-propiolactone to producepolypropiolactone. Depending on the type of polymerization reactorsselected and the configuration of such reactors, as well as theoperating conditions (e.g., operating temperature, operating pressure,and residence time) and choice of polymerization catalysts used, theextent of conversion of the β-propiolactone may be controlled. In somevariations, operating temperature is the average temperature of thecontents of the reactor.

In some variations, partial conversion of β-propiolactone topolypropiolactone is achieved, and bPL recycle unit 220 is configured torecycle at least a portion of unreacted β-propiolactone topolypropiolactone production system/production process 210. In othervariations, complete conversion of β-propiolactone to polypropiolactoneis achieved. The polypropiolactone product stream produced frompolypropiolactone production system/production process 210 is fedglacial acrylic acid production system/production process 250, which isconfigured to produce glacial acrylic acid from the polypropiolactone.Ion removal units 230 and 260 are present to remove at cationic and/oranionic carbonylation catalyst species that may be carried over from theupstream carbonylation reaction in the β-propiolactone productionsystem/production process (not depicted in FIG. 2). For example, whenthe carbonylation catalyst is a cobalt-aluminum compound, cobalt andaluminum species may be removed by ion removal units 230 and 260. Theionic species isolated by the ion removal units may be disposed usingunit 270, or regenerated in unit 280 to produce an active carbonylationcatalyst that may be recycled into the β-propiolactone productionsystem/production process.

In some variations, unit 240 is configured to receive thepolypropiolactone product stream (e.g., in liquid form) frompolypropiolactone production system/production process 210, and isconfigured to pelletize, extrude, flake, or granulate thepolypropiolactone product stream.

It should be understood, however, that FIG. 2 provides one exemplaryconfiguration of these unit operations. In other variations, one or moreof the unit operations depicted in FIG. 2 may be added, combined oromitted, and the order of the unit operations may be varied as well.

With reference again to FIG. 1, the polypropiolactone productionsystem/production process is configured to produce polypropiolactone bypolymerizing β-propiolactone in the presence of a polymerizationcatalyst. While FIG. 1 depicts the use of a single plug flow reactor forthe polymerization of β-propiolactone to produce polypropiolactone,other reactor types and reactor configurations may be employed.

In some embodiments, the polypropiolactone production system/productionprocess includes a β-propiolactone, a polymerization initiator orcatalyst source, and at least one polymerization reactor.

BPL Source

With reference again to FIGS. 6-13, the bPL entering thepolypropiolactone production system/production process may be purifiedbPL from the bPL purification train or recycled bPL from thepolymerization reactor, or a combination thereof.

In some embodiments, the inlet to the polymerization process can includeat least about 2000 kg/hr bPL, at least about 2500 kg/hr bPL, at leastabout 3000 kg/hr bPL, at least about 3086 kg/hr bPL, at least about 3500kg/hr bPL, at least about 3638 kg/hr bPL, at least about 4000 kg/hr bPL,at least about 5000 kg/hr bPL, at least about 1000 kg/hr bPL, at leastabout 20000 kg/hr bPL, or at least about 35000 kg/hr bPL. In someembodiments, the inlet to the polymerization process can include about2000 kg/hr bPL, about 2500 kg/hr bPL, about 3000 kg/hr bPL, about 3500kg/hr bPL, about 3638 kg/hr bPL, about 4000 kg/hr bPL, about 5000 kg/hrbPL, about 1000 kg/hr bPL, about 20000 kg/hr bPL, or about 35000 kg/hrbPL. In some embodiments, the inlet to the polymerization process caninclude between about 2000 kg/hr bPL and about 3500 kg/hr bPL, betweenabout 2500 kg/hr bPL and about 3500 kg/hr bPL, between about 3000 kg/hrbPL and about 3500 kg/hr bPL, between about 2000 kg/hr bPL and about35000 kg/hr bPL, between about 2500 kg/hr bPL and about 35000 kg/hr bPL,or between about 3000 kg/hr bPL and about 35000 kg/hr bPL. In someembodiments, the inlet to the polymerization process can include atleast about 25 kmol/hr bPL, at least about 30 kmol/hr bPL, at leastabout 40 kmol/hr bPL, at least about 42 kmol/hr bPL, or at least about50 kmol/hr bPL. In some embodiments, the mass fraction of bPL in theinlet to the polymerization process can be at least about 0.90, at leastabout at least about 0.95, at least about 0.98, at least about 0.99, andat least about 0.993. In some embodiments, the mole fraction of bPL inthe inlet to the polymerization process can be at least about 0.90, atleast about at least about 0.95, at least about 0.98, at least about0.99, and at least about 0.995. The remainder of the production streamentering the polymerization process can include secondary reactionproducts such as succinic anhydride (in mole fraction of at most about0.015, at most about 0.01, or at most about 0.004) and left over solvent(e.g., THF) and leftover carbonylation catalyst (in at most about 1000ppm). In some variations, the remainder of the production streamentering the polymerization process can include carbonylation catalystcomponents (in at most about 1000 ppm).

In some variations, the production stream entering the polymerizationprocess further comprises other compounds, such as carbonylationcatalyst or components thereof. For example, in some embodiments, theproduction stream further comprises cobalt or aluminum, or a combinationthereof, from the carbonylation catalyst.

Carbonylation catalyst components may include, for example, compoundsproduced by degradation of the catalyst, compounds used to produce thecatalyst, metals or metal ions which were part of the catalyst, anyorganic compounds which were part of the catalyst, metal carbonyls ormetal complexes which were part of the catalyst. For example, in someembodiments, carbonylation catalyst components are carbonyl cobaltate,aluminum salen compounds, aluminum porphyrin compounds, aluminumsalophen compounds, cobalt or cobalt ions, or aluminum or aluminum ions,or any combinations thereof.

In certain variations, the production stream entering the polymerizationprocess comprises cobalt. In some embodiments, the cobalt is Co⁻¹, Co,Co⁺, Co²⁺, or Co³⁺, or a combination thereof. In some embodiments, theproduction stream has a cobalt concentration between 0.001 mM and 1 mM,0.001 mM and 0.5 mM, between 0.001 mM and 0.05 mM, between 0.005 mM and0.02 mM, or between 0.007 mM and 0.015 mM.

In certain variations, the production stream entering the polymerizationprocess comprises aluminum. In some embodiments, the concentration ofaluminum in the production stream is between 0.001 mM and 1 mM, 0.001 mMand 0.5 mM, between 0.001 mM and 0.05 mM, between 0.005 mM and 0.02 mM,or between 0.007 mM and 0.015 mM. In certain variations, the productionstream entering the polymerization process contains less than 1 ppmcobalt and less than 1 ppm aluminum.

In some embodiments, the inlet to the polymerization process can alsoinclude a polymerization catalyst, for example, if the polymerizationreaction is a homogenous polymerization reaction. The production streamentering the polymerization process can be the heavy (i.e., bottoms)stream from the BPL Purification system (e.g., BPL distillation system).In some embodiments, the production stream entering the polymerizationprocess can have a temperature between about 30-120° C., between about50-110° C., or about 70° C. In some embodiments, the production streamentering the polymerization process can be at a pressure of at leastabout 0.05 bar, at least about 0.1 bar, at least about 5 bar, at leastabout 10 bar, at least about 15 bar, or at least about 20 bar. In someembodiments, production stream entering the polymerization process isbetween 0.05 bar and 20 bar, between 0.1 bar and 20 bar, between 5 barand 15 bar, or between 10 bar and 20 bar.

In some variations, the mole ratio of bPL feed rate to thepolymerization initiator feed rate entering the polymerization processis from 500 to 20,000, from 1,000 to 10,000, from 2,000 to 9,000, from3,000 to 8,000, from 5,000 to 7,000, from 1,000 to 110,000, from 5,000to 110,000, from 25,000 to 110,000, from 50,000 to 110,000, or from75,000 to 110,000. In one embodiment, mole ratio of bPL feed rate to thepolymerization catalyst feed rate entering the polymerization process isfrom 1,000 to 9,000.

In some variations, bPL from the bPL purification process and bPLrecycled from the polymerization process both enter the polymerizationprocess. In certain embodiments, the weight ratio of recycled bPL to bPLfrom the bPL Purification process is from 0 to 0.01:0.99, from 0.4:0.6to 0.1:0.9, from 0.5:0.5 to 0.15:0.85, from 0.35:0.65 to 0.1:0.9, orfrom 0.25:0.75 to 0.15:0.85.

Other Feed Sources

The polymerization process may further include other feed sources. Forexample, in one variation, the polymerization system further includes apolymerization initiator source, and the reactor is configured toreceive a polymerization initiator from such source. In some variations,the polymerization initiator is a nucleophile.

Polymerization Conditions

In certain embodiments, conversion of bPL to PPL is performed in acontinuous flow format. In certain embodiments, conversion of bPL to PPLis performed in a continuous flow format in the gas phase. In certainembodiments, conversion of bPL to PPL is performed in a continuous flowformat in the liquid phase. In certain embodiments, conversion of bPL toPPL is performed in a liquid phase in a batch or semi-batch format.Conversion of bPL to PPL may be performed under a variety of conditions.In certain embodiments, the reaction may be performed in the presence ofone or more catalysts that facilitate the transformation of the bPL toPPL.

In some embodiments, the production stream entering the polymerizationprocess is a gas or a liquid. The conversion of bPL to PPL in thepolymerization process may be performed in either the gas phase or theliquid phase and may be performed neat, or in the presence of a carriergas, solvent, or other diluent.

In certain variations, the operating temperature of the polymerizationreactor is maintained at or below the pyrolysis temperature ofpolypropiolactone. In some embodiments, the temperature of the reactionzone is maintained at or below about 150° C. In some embodiments, theoperating temperature of the polymerization reactor is maintained atabout 0° C. to about 200° C. In some embodiments, the operatingtemperature of the polymerization reactor is maintained at about 25° C.to about 200° C. In some embodiments, the operating temperature of thepolymerization reactor is maintained at about 50° C. to about 150° C. Insome embodiments, the operating temperature of the polymerizationreactor is maintained at about 70° C. to about 150° C. In someembodiments, the operating temperature of the polymerization reactor ismaintained at about 100° C. to about 150° C. In some embodiments, theoperating temperature of the polymerization reactor is maintained atabout 0° C. to about 100° C. In some embodiments, the operatingtemperature of the polymerization reactor is maintained at about 50° C.to about 100° C. In some variations, operating temperature is theaverage temperature of the contents of the reactor.

In some variations, the polymerization reactor is configured to producePPL with a residence time from 1 second to 10 hours, from 1 second to 3hours, from 1 min to 2 hours, from 1.5 min to 90 min, from 2 min to 75min, from 2 min to 60 min, from 2 min to 45 min, from 3 min to 30 min,or from 4 min to 15 min. In one embodiment the residence time of thereaction mixture is from 2 min to 90 min. In certain variations,residence time refers to the length of time a material spends in avessel (for example, a reaction vessel). It may be calculated byspecifying the volumetric flow rate of material and active volume of thevessel which the material is contained.

In some variations, the polymerization reactor is configured to producePPL at an operating pressure from 0.01 bar to 100 bar, from 0.01 bar to50 bar, from 0.1 bar to 30 bar, from 1 bar to 20 bar, from 2 bar to 15bar, from 3 bar to 10 bar, from 0.01 bar to 15 bar, from 0.01 bar to 10bar, from 0.1 bar to 5 bar, or from 0.1 bar to 2 bar. In someembodiments, the polymerization reactor is a CSTR and operating pressurein the reactor is from 0.1 bar to 5 bar. In other embodiments, thepolymerization reactor is a PFR and the operating pressure in thereactor is from 1 bar to about 20 bar. In still other embodiments, thepolymerization reactor is a loop reactor and the operating pressure inthe reactor is from 1 bar to about 20 bar.

Homogeneous Catalysts and Initiators

Any suitable polymerization initiators and/or catalysts may be used toconvert the BPL product stream entering the PPL productionsystem/production process into a PPL product stream. In someembodiments, the polymerization initiator or catalyst is homogenous withthe polymerization reaction mixture. Any suitable homogeneouspolymerization initiator or catalyst capable of converting theproduction stream to the PPL product stream may be used in the methodsdescribed herein.

Catalysts suitable for the ring-opening polymerization step of themethods disclosed herein are disclosed, for example, in: Journal of theAmerican Chemical Society (2002), 124(51), 15239-15248 Macromolecules,vol. 24, No. 20, pp. 5732-5733, Journal of Polymer Science, Part A-1,vol. 9, No. 10, pp. 2775-2787; Inoue, S., Y. Tomoi, T. Tsuruta & J.Furukawa; Macromolecules, vol. 26, No. 20, pp. 5533-5534;Macromolecules, vol. 23, No. 13, pp. 3206-3212; Polymer Preprints(1999), 40(1), 508-509; Macromolecules, vol. 21, No. 9, pp. 2657-2668;and Journal of Organometallic Chemistry, vol. 341, No. 1-3, pp. 83-9;and in U.S. Pat. Nos. 3,678,069, 3,169,945, 6,133,402; 5,648,452;6,316,590; 6,538,101; and 6,608,170. The entirety of each of which ishereby incorporated herein by reference.

The polymerization process may further comprise a polymerizationinitiator including but not limited to amines, polyamines, phosphinesamongst others. Further, a variety of polymerization initiators may beused in the polymerization process, including by not limited tocarbonates of alkali- and alkaline earth metals.

In certain embodiments, suitable polymerization initiators includecarboxylate salts of metal ions or organic cations.

In certain embodiments, a polymerization initiator is combined with theproduction stream containing bPL. In certain embodiments, the molarratio of the polymerization initiator to the bPL in the productionstream is about 1:15000. In certain embodiments, the molar ratio ofpolymerization intiator:bPL is about 1:100, 1:10000, 1:1000, 1:20000 ora range including any two of these ratios.

In certain embodiments, where the polymerization initiator comprises acarboxylate salt, the carboxylate has a structure such that uponinitiating polymerization of bPL, the polymer chains produced have anacrylate chain end. In certain embodiments, the carboxylate ion on apolymerization initiator is the anionic form of a chain transfer agentused in the polymerization process.

In certain embodiments, the carboxylate salt of the polymerizationinitiator is a salt of (i.e., the anionic form) a compound of Formula(A):

or a mixture of any two or more of these, where p is from 0 to 9. Incertain embodiments, p is from 0 to 5. In certain embodiments, thecarboxylate salt of the polymerization initiator is an acrylate salt(i.e. compound of Formula (A) where p=0).

In certain embodiments, the carboxylate salt of the polymerizationinitiator is a salt of an acrylic acid dimer,

In certain embodiments, the carboxylate salt of the polymerizationinitiator is a salt of an acrylic acid trimer,

In certain embodiments, where the polymerization initiator comprises acarboxylate salt, the carboxylate is the anionic form of a C₁₋₄₀carboxylic acid. In certain embodiments, the carboxylate salt can be asalt of a polycarboxylic acid (e.g. a compound having two or morecarboxylic acid groups). In certain embodiments, the carboxylatecomprises the anion of a C₁₋₂₀ carboxylic acid. In certain embodiments,the carboxylate comprises the anion of a C₁₋₁₂ carboxylic acid. Incertain embodiments, the carboxylate comprises the anion of a C₁₋₈carboxylic acid. In certain embodiments, the carboxylate comprises theanion of a C₁₋₄ carboxylic acid. In certain embodiments, the carboxylatecomprises the anion of an optionally substituted benzoic acid. Incertain embodiments, the carboxylate is selected from the groupconsisting of: formate, acetate, propionate, valerate, butyrate, C₅₋₁₀aliphatic carboxylate, and C₁₀₋₂₀ aliphatic carboxylate.

As noted, in certain embodiments, the polymerization initiator comprisesa carboxylate salt of an organic cation. In certain embodiments, thepolymerization initiator comprises a carboxylate salt of a cationwherein the positive charge is located at least partially on a nitrogen,sulfur, or phosphorus atom. In certain embodiments, the polymerizationinitiator comprises a carboxylate salt of a nitrogen cation. In certainembodiments, the polymerization initiator comprises a carboxylate saltof a cation selected from the group consisting of: ammonium, amidinium,guanidinium, a cationic form of a nitrogen heterocycle, and anycombination of two or more of these. In certain embodiments, thepolymerization initiator comprises a carboxylate salt of a phosphoruscation. In certain embodiments, the polymerization initiator comprises acarboxylate salt of a cation selected from the group consisting of:phosphonium and phosphazenium. In certain embodiments, thepolymerization initiator comprises a carboxylate salt of asulfur-containing cation. In certain embodiments, the polymerizationinitiator comprises a sulfonium salt.

In certain embodiments, the polymerization initiator comprises acarboxylate salt of a protonated amine:

wherein:

each R¹ and R² is independently hydrogen or an optionally substitutedradical selected from the group consisting of C₁₋₂₀ aliphatic; C₁₋₂₀heteroaliphatic; a 3- to 8-membered saturated or partially unsaturatedmonocyclic carbocycle; a 7- to 14-membered saturated or partiallyunsaturated polycyclic carbocycle; a 5- to 6-membered monocyclicheteroaryl ring having 1-4 heteroatoms independently selected fromnitrogen, oxygen, or sulfur; an 8- to 14-membered polycyclic heteroarylring having 1-5 heteroatoms independently selected from nitrogen,oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturatedmonocyclic heterocyclic ring having 1-3 heteroatoms independentlyselected from nitrogen, oxygen, or sulfur; a 6- to 14-membered saturatedor partially unsaturated polycyclic heterocycle having 1-5 heteroatomsindependently selected from nitrogen, oxygen, or sulfur; phenyl; or an8- to 14-membered polycyclic aryl ring; wherein R¹ and R² can be takentogether with intervening atoms to form one or more optionallysubstituted rings optionally containing one or more additionalheteroatoms;

each R³ is independently hydrogen or an optionally substituted radicalselected from the group consisting of C₁₋₂₀ aliphatic; C₁₋₂₀heteroaliphatic; a 3- to 8-membered saturated or partially unsaturatedmonocyclic carbocycle; a 7- to 14-membered saturated or partiallyunsaturated polycyclic carbocycle; a 5- to 6-membered monocyclicheteroaryl ring having 1-4 heteroatoms independently selected fromnitrogen, oxygen, or sulfur; an 8- to 14-membered polycyclic heteroarylring having 1-5 heteroatoms independently selected from nitrogen,oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturatedmonocyclic heterocyclic ring having 1-3 heteroatoms independentlyselected from nitrogen, oxygen, or sulfur; a 6- to 14-membered saturatedor partially unsaturated polycyclic heterocycle having 1-5 heteroatomsindependently selected from nitrogen, oxygen, or sulfur; phenyl; or an8- to 14-membered polycyclic aryl ring; wherein an R³ group can be takenwith an R¹ or R² group to form one or more optionally substituted rings.

In certain embodiments where the polymerization initiator comprises acarboxylate salt of a protonated amine, the protonated amine is selectedfrom the group consisting of:

In certain embodiments, the polymerization initiator comprises acarboxylate salt of a quaternary ammonium salt:

wherein:

each R¹, R² and R³ is described above; and

each R⁴ is independently hydrogen or an optionally substituted radicalselected from the group consisting of C₁₋₂₀ aliphatic; C₁₋₂₀heteroaliphatic; a 3- to 8-membered saturated or partially unsaturatedmonocyclic carbocycle; a 7- to 14-membered saturated or partiallyunsaturated polycyclic carbocycle; a 5- to 6-membered monocyclicheteroaryl ring having 1-4 heteroatoms independently selected fromnitrogen, oxygen, or sulfur; an 8- to 14-membered polycyclic heteroarylring having 1-5 heteroatoms independently selected from nitrogen,oxygen, or sulfur; a 3- to 8-membered saturated or partially unsaturatedmonocyclic heterocyclic ring having 1-3 heteroatoms independentlyselected from nitrogen, oxygen, or sulfur; a 6- to 14-membered saturatedor partially unsaturated polycyclic heterocycle having 1-5 heteroatomsindependently selected from nitrogen, oxygen, or sulfur; phenyl; or an8- to 14-membered polycyclic aryl ring; wherein an R⁴ group can be takenwith an R¹, R² or R³ group to form one or more optionally substitutedrings.

In certain embodiments, the polymerization initiator comprises acarboxylate salt of a guanidinium group:

wherein each R¹ and R² is independently as defined above and describedin classes and subclasses herein. In certain embodiments, each R¹ and R²is independently hydrogen or C₁₋₂₀ aliphatic. In certain embodiments,each R¹ and R² is independently hydrogen or C₁₋₁₂ aliphatic. In certainembodiments, each R¹ and R² is independently hydrogen or C₁₋₂₀heteroaliphatic. In certain embodiments, each R¹ and R² is independentlyhydrogen or phenyl. In certain embodiments, each R¹ and R² isindependently hydrogen or 8- to 10-membered aryl. In certainembodiments, each R¹ and R² is independently hydrogen or 5- to10-membered heteroaryl. In certain embodiments, each R¹ and R² isindependently hydrogen or 3- to 7-membered heterocyclic. In certainembodiments, one or more of R¹ and R² is optionally substituted C₁₋₁₂aliphatic.

In certain embodiments, any two or more R¹ or R^(e) groups are takentogether with intervening atoms to form one or more optionallysubstituted carbocyclic, heterocyclic, aryl, or heteroaryl rings. Incertain embodiments, R¹ and R² groups are taken together to form anoptionally substituted 5- or 6-membered ring. In certain embodiments,three or more R′ and/or R² groups are taken together to form anoptionally substituted fused ring system.

In certain embodiments, an R¹ and R² group are taken together withintervening atoms to form a compound selected from:

wherein each R¹ and R² is independently as defined above and describedin classes and subclasses herein, and Ring G is an optionallysubstituted 5- to 7-membered saturated or partially unsaturatedheterocyclic ring.

It will be appreciated that when a guanidinium cation is depicted as

all such resonance forms are contemplated and encompassed by the presentdisclosure. For example, such groups can also be depicted as

In specific embodiments, a guanidinium cation is selected from the groupconsisting of:

In certain embodiments, a polymerization initiator comprises acarboxylate salt of a sulfonium group or an arsonium group:

wherein each of R¹, R², and R³ are as defined above and described inclasses and subclasses herein.

In specific embodiments, an arsonium cation is selected from the groupconsisting of:

In certain embodiments, a polymerization initiator comprises acarboxylate salt of an optionally substituted nitrogen-containingheterocycle. In certain embodiments, the nitrogen-containing heterocycleis an aromatic heterocycle. In certain embodiments, the optionallysubstituted nitrogen-containing heterocycle is selected from the groupconsisting of: pyridine, imidazole, pyrrolidine, pyrazole, quinoline,thiazole, dithiazole, oxazole, triazole, pyrazolem, isoxazole,isothiazole, tetrazole, pyrazine, thiazine, and triazine.

In certain embodiments, a nitrogen-containing heterocycle includes aquaternarized nitrogen atom. In certain embodiments, anitrogen-containing heterocycle includes an iminium moiety such as

In certain embodiments, the optionally substituted nitrogen-containingheterocycle is selected from the group consisting of pyridinium,imidazolium, pyrrolidinium, pyrazolium, quinolinium, thiazolium,dithiazolium, oxazolium, triazolium, isoxazolium, isothiazolium,tetrazolium, pyrazinium, thiazinium, and triazinium.

In certain embodiments, a nitrogen-containing heterocycle is linked to ametal complex via a ring nitrogen atom. In certain embodiments, a ringnitrogen to which the attachment is made is thereby quaternized, and Incertain embodiments, linkage to a metal complex takes the place of anN—H bond and the nitrogen atom thereby remains neutral. In certainembodiments, an optionally substituted N-linked nitrogen-containingheterocycle is a pyridinium derivative. In certain embodiments,optionally substituted N-linked nitrogen-containing heterocycle is animidazolium derivative. In certain embodiments, optionally substitutedN-linked nitrogen-containing heterocycle is a thiazolium derivative. Incertain embodiments, optionally substituted N-linked nitrogen-containingheterocycle is a pyridinium derivative.

In certain embodiments, a polymerization initiator comprises acarboxylate salt of

In certain embodiments, ring A is an optionally substituted, 5- to10-membered heteroaryl group. In certain embodiments, Ring A is anoptionally substituted, 6-membered heteroaryl group. In certainembodiments, Ring A is a ring of a fused heterocycle. In certainembodiments, Ring A is an optionally substituted pyridyl group.

In specific embodiments, a nitrogen-containing heterocyclic cation isselected from the group consisting of:

In certain embodiments, a polymerization initiator comprises acarboxylate salt of

where each R¹, R², and R³ is independently as defined above anddescribed in classes and subclasses herein.

In certain embodiments, a polymerization initiator comprises acarboxylate salt of

wherein each R¹ and R² is independently as defined above and describedin classes and subclasses herein.

In certain embodiments, a polymerization initiator comprises acarboxylate salt of

wherein each R¹, R², and R³ is independently as defined above anddescribed in classes and subclasses herein.

In certain embodiments, a polymerization initiator comprises acarboxylate salt of

wherein each of R¹, R², R⁶, and R⁷ is as defined above and described inclasses and subclasses herein.

In certain embodiments, R⁶ and R⁷ are each independently an optionallysubstituted group selected from the group consisting of C₁₋₂₀ aliphatic;C₁₋₂₀ heteroaliphatic; phenyl, and 8-10-membered aryl. In certainembodiments, R⁶ and R⁷ are each independently an optionally substitutedC₁₋₂₀ aliphatic. In certain embodiments, R⁶ and R⁷ are eachindependently an optionally substituted C₁₋₂₀ heteroaliphatic having. Incertain embodiments, R⁶ and R⁷ are each independently an optionallysubstituted phenyl or 8-10-membered aryl. In certain embodiments, R⁶ andR⁷ are each independently an optionally substituted 5- to 10-memberedheteroaryl. In certain embodiments, R⁶ and R⁷ can be taken together withintervening atoms to form one or more rings selected from the groupconsisting of: optionally substituted C₃-C₁₄ carbocycle, optionallysubstituted C₃-C₁₄ heterocycle, optionally substituted C₆-C₁₀ aryl, andoptionally substituted 5- to 10-membered heteroaryl. In certainembodiments, R⁶ and R⁷ are each independently an optionally substitutedC₁₋₆ aliphatic. In certain embodiments, each occurrence of R⁶ and R⁷ isindependently methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl,octyl, or benzyl. In certain embodiments, each occurrence of R⁶ and R⁷is independently perfluoro. In certain embodiments, each occurrence ofR⁶ and R⁷ is independently —CF₂CF₃.

In certain embodiments, a polymerization initiator comprises acarboxylate salt of

wherein each R¹ and R² is independently as defined above and describedin classes and subclasses herein.

In certain embodiments, a polymerization initiator comprises acarboxylate salt

wherein each R¹, R², and R³ is independently as defined above anddescribed in classes and subclasses herein.

In certain embodiments, a cation is

wherein each R¹ and R² is independently as defined above and describedin classes and subclasses herein.

In certain embodiments, a polymerization initiator comprises acarboxylate salt of

wherein each R¹ and R² is independently as defined above and describedin classes and subclasses herein.

In certain embodiments, a polymerization initiator comprises acarboxylate salt of

wherein each R¹, R², and R³ is independently as defined above anddescribed in classes and subclasses herein.

In certain embodiments, a polymerization initiator comprises acarboxylate salt of

wherein each R¹ and R² is independently as defined above and describedin classes and subclasses herein. In certain embodiments, suitableinitiator include transition metal compounds. In certain embodiments,suitable catalysts include acid catalysts. In certain embodiments, thecatalyst is a heterogeneous catalyst.

In some embodiments, the homogeneous polymerization initiator is aquaternary ammonium salt (for example, tetrabutylammonium (TBA)acrylate, TBA acetate, trimethylphenylammonium acrylate, ortrimethylphenylammonium acetate) or a phosphine (for example,tetraphenyl phosphonium acrylate).

In some embodiments, the catalyst is tetrabutylammonium acrylate, sodiumacrylate, potassium acrylate, iron chloride, tetrabutylammonium acetate,trimethylphenylammonium acrylate, trimethylphenylammonium acetate, ortetraphenyl phosphonium acrylate.

With reference to FIG. 4A, the polymerization catalyst in the firstreactor (408) and the additional polymerization initiator in the secondreactor (410) may be the same or different. For example, in someembodiments, wherein the same initiator is used in both reactors,concentration of initiator is not the same in each reactor.

In some embodiments, the homogeneous polymerization initiator is addedto a polymerization reactor as a liquid. In other embodiments it isadded as a solid, which then becomes homogeneous in the polymerizationreaction. In some embodiments where the polymerization initiator isadded as a liquid, the polymerization initiator may be added to thepolymerization reactor as a melt or in any suitable solvent. Forexample, in some variations GAA, molten PPL or bPL is used as a solvent.

In some embodiments, the solvent for the polymerization initiator isselected such that the initiator is soluble, the solvent does notcontaminate the product polymer, and the solvent is dry. In somevariations, the polymerization initiator solvent is GAA, molten PPL, orbPL. In certain variations, solid PPL is added to a polymerizationreactor, heated above room temperature until liquid, and used as thepolymerization initiator solvent. In other embodiments, bPL is added tothe polymerization reactor, cooled below room temperature until liquid,and used as the polymerization initiator solvent.

In some variations, the solid or liquid polymerization initiator (as amelt or as a solution in a suitable solvent) is prepared in onelocation, then shipped to a second location where it is used in thepolymerization reactor. In other embodiments, the solid or liquidpolymerization initiator (as a melt or as a solution in a suitablesolvent) is prepared at the location of the polymerization reactor (forexample, to reduce exposure to moisture and/or oxygen).

A solid or liquid polymerization initiator (as a melt or as a solutionin a suitable solvent) may be pumped into a stirred holding tank ordirectly into the polymerization reactor.

In some variations, the liquid initiator and/or initiator precursors aredispensed from a shipping vessel/container into an intermediate, inertvessel to be mixed with suitable solvent, and then the initiatorsolution is fed to the reactor or a pre-mix tank. The initiatorpreparation system and the connections may be selected in such a way toensure that the initiator or precursors are not contacted by ambientatmosphere.

In some variations, the polymerization reactor is a PFR, the solid orliquid initiator (as a melt or as a solution in a suitable solvent) andbPL are fed to a small stirred tank and then the mixture is fed to thePFR. In other embodiments, the bPL and the liquid catalyst are fed to apre-mixer installed at the inlet of the PFR. In yet another embodiment,the PFR has a static mixer, the reaction occurs on the shell side of thereactor, and the solid or liquid initiator and bPL are introduced at theinlet of the reactor and the static mixer elements mix the initiator andbPL. In still another embodiments, the PFR has a static mixer, thereaction occurs on the shell side of the reactor, and the solid orliquid initiator is introduced into the PFR using metering pumps/feedersat multiple locations distributed along the lengths of the reactor.

In some embodiments, the homogeneous polymerization initiator isdelivered to the location of the polymerization reactor as a solid (forexample, solid Al(TPP)Et, solid sodium acrylate, solid potassiumacrylate, solid sodium acetate, solid potassium acetate, or solid TBAacrylate), the solid initiator is unpacked and loaded in hoppers underinert conditions (CO or inert gas), and the solids from hoppers can befed directly into the polymerization reactor, or be mixed with bPL priorto the reactor, or be metered into a suitable solvent before pumpinginto the polymerization reactors or mixing tanks.

Heterogeneous System

Any suitable polymerization catalyst may be used in the polymerizationprocess to convert the production stream entering the polymerizationprocess to the PPL product stream. In some embodiments, thepolymerization catalyst is heterogeneous with the polymerizationreaction mixture. Any suitable heterogeneous polymerization catalystcapable of polymerizing bPL in the production stream to produce the PPLproduct stream may be used in the methods described herein.

In some embodiments, the heterogeneous polymerization catalyst comprisesany of the homogeneous polymerization catalysts described above,supported on a heterogeneous support. Suitable heterogeneous supportsmay include, for example, amorphous supports, layered supports, ormicroporous supports, or any combination thereof. Suitable amorphoussupports may include, for example, metal oxides (such as aluminas orsilicas) or carbon, or any combination thereof. Suitable layeredsupports may include, for example, clays. Suitable microporous supportsmay include, for example, zeolites (such as molecular sieves) orcross-linked functionalized polymers. Other suitable supports mayinclude, for example, glass surfaces, silica surfaces, plastic surfaces,metal surfaces including zeolites, surfaces containing a metallic orchemical coating, membranes (comprising, for example, nylon,polysulfone, silica), micro-beads (comprising, for example, latex,polystyrene, or other polymer), and porous polymer matrices (comprising,for example, polyacrylamide, polysaccharide, polymethacrylate).

In some variations, the heterogeneous polymerization catalyst comprisesthe carboxylate salt of any of the homogeneous polymerization catalystsdescribed above, wherein the carboxylate is heterogeneous. For example,in certain embodiments, the carboxylate of the polymerization catalystis a compound of Formula (D):

where p is from 0 to 9 and R^(a) is a non-volatile moiety. The term“non-volatile moiety,” as used herein, refers to a moiety or material towhich a carboxylate can be attached, and that renders the carboxylate(e.g., when p=0) non-volatile to pyrolysis conditions. In someembodiments, a non-volatile moiety is selected from the group consistingof glass surfaces, silica surfaces, plastic surfaces, metal surfacesincluding zeolites, surfaces containing a metallic or chemical coating,membranes (comprising, for example, nylon, polysulfone, silica),micro-beads (comprising, for example, latex, polystyrene, or otherpolymer), and porous polymer matrices (comprising, for example,polyacrylamide, polysaccharide, polymethacrylate). In some embodiments,the non-volatile moiety has a molecular weight above 100, 200, 500, or1000 g/mol. In some embodiments, the non-volatile moiety is part of afixed or packed bed system. In some embodiments, the non-volatile moietyis part of a fixed or packed bed system comprising pellets (e.g.,zeolite). In certain embodiments, p is from 0 to 5. In certainembodiments, the carboxylate salt of the polymerization catalyst is anacrylate salt (i.e., of compound of Formula (D) where p=0).

In some embodiments, the heterogeneous polymerization catalyst is asolid-supported quaternary ammonium salt (for example,tetrabutylammonium (TBA) acrylate, TBA acetate, trimethylphenylammoniumacrylate, or trimethylphenylammonium acetate) or a phosphine (forexample, tetraphenyl phosphonium acrylate).

In some embodiments, the catalyst is solid-supported tetrabutylammoniumacrylate, iron chloride, TBA acetate, trimethylphenylammonium acrylate,trimethylphenylammonium acetate, or tetraphenyl phosphonium acrylate.

In certain embodiments, conversion of the production stream entering thepolymerization process to the PPL product stream utilizes a solidcarboxylate catalyst and the conversion is conducted at least partiallyin the gas phase. In certain embodiments, the solid carboxylate catalystin the polymerization process comprises a solid acrylic acid catalyst.In certain embodiments, the production stream enters the polymerizationprocess as a liquid and contacted with a solid carboxylate catalyst toform the PPL product stream. In other embodiments, the production streamenters the polymerization process as a gas and contacted with a solidcarboxylate catalyst to form the PPL product stream.

In some variations, the polymerization catalyst is a heterogeneouscatalyst bed. Any suitable resin may be used for such a heterogeneouscatalyst bed. In one embodiment, the polymerization catalyst is aheterogeneous catalyst bed packed in a tubular reactor. In someembodiments, the polymerization reactor system comprises a plurality ofheterogeneous catalyst beds, wherein at least one catalyst bed is beingused in the polymerization reactor, and at least one catalyst bed is notbeing used in the polymerization reactor at the same time. For example,the catalyst bed not actively being used may be being regenerated forlater use, or may be stored as a back-up catalyst bed in case ofcatalyst failure of the actively used bed. In one embodiment, thepolymerization reactor system comprises three heterogeneous catalystbeds, wherein one catalyst bed is being used in the polymerizationreactor, one catalyst bed is being regenerated, and one catalyst bed isbeing stored as a back-up in case of catalyst failure.

In some variations, the heterogeneous polymerization catalyst isprepared in one location, then shipped to a second location where it isused in the polymerization reactor. In other embodiments, theheterogeneous polymerization catalyst is prepared at the location of thepolymerization reactor (for example, to reduce exposure to moistureand/or oxygen).

Solvents

In some embodiments, the polymerization process does not includesolvent. In other embodiments, the polymerization process does includeone or more solvents. Suitable solvents can include, but are not limitedto: hydrocarbons, ethers, esters, ketones, nitriles, amides, sulfones,halogenated hydrocarbons, and the like. In certain embodiments, thesolvent is selected such that the PPL product stream is soluble in thereaction medium.

Without wishing to be bound by any particular theory, it is believedthat solvents comprising Lewis bases of low to moderate polarity improvethe performance of the polymerization reaction. Thus, in certainembodiments, a polymerization solvent comprises a Lewis base and is lesspolar than 1,3-dioxane (ε=dielectric constant at 20° C.=13.6). Incertain embodiments, a polymerization solvent comprises a Lewis base andis less polar than ortho-difluorobenzene (ε=13). In certain embodiments,a polymerization solvent comprises a Lewis base and is less polar thanmetadifluorobenzene (ε=5). In certain embodiments, a polymerizationsolvent comprises a Lewis base with substantially the same polarity as1,4-dioxane (ε=2.2). In some embodiments, a polymerization solvent isless polar than a carbonylation solvent as measured by dielectricconstant. In some embodiments, a polymerization solvent has a dielectricconstant at 20° C. of less than about 13.6, less than about 13, or lessthan about 5.

For example, with reference to polymerization process depicted in FIGS.4A and 4B, reactors 408 and/or 410 may be configured to receive solvent.For example, in one variation, polymerization process may furtherinclude a solvent source configured to feed solvent into reactors 408and 410. In another variation, the bPL from production stream 402 may becombined with solvent to form the production stream containing bPL fedinto reactor 408. In yet another variation, the polymerization catalystfrom polymerization catalyst sources 404 and/or 406 may be combined witha solvent to form polymerization catalyst streams fed into the reactors.

Polymerization Reactors

The one or more polymerization reactors in the polymerization processmay be any suitable polymerization reactors for the production of thePPL product stream from the production stream entering thepolymerization process. For example, the polymerization reactor may be aCSTR, loop reactor, or plug flow reactor, or a combination thereof. Insome embodiments, the polymerization process comprises a single reactor,while in other embodiments, the polymerization process comprises aplurality of reactors. In some variations, the bPL is completelyconverted to PPL in a polymerization reactor. In other variations, thebPL is not completely converted to PPL in a polymerization reactor, andthe PPL stream exiting the polymerization reactor comprises unreactedbPL. In certain variations, the PPL stream comprising unreacted bPL isdirected to a bPL/PPL separator to remove the bPL from the PPL. The bPLmay then be recycled back into the polymerization reactor, as described,for example, in FIGS. 7, 9, 11 and 13 above.

In certain variations, the polymerization process comprises two reactorsin series, wherein the purified bPL stream enters the first reactor andundergoes incomplete polymerization to produce a first polymerizationstream comprising PPL and unreacted bPL, the first polymerization streamexits the outlet of the first reactor and enters the inlet of the secondreactor to undergo additional polymerization. In some variations, theadditional polymerization completely converts the bPL to PPL, and thePPL product stream exits the outlet of the second polymerizationreactor.

In other variations, the additional polymerization incompletely convertsthe bPL to PPL, and the PPL product stream exiting the outlet of thesecond polymerization reactor comprises PPL and unreacted bPL. Incertain variations, the PPL product stream enters a BPL/PPL separator toremove unreacted bPL from the PPL product stream. In certain variations,the unreacted bPL is recycled back into the polymerization process. Forexample, in some variations, the unreacted bPL is recycled to the firstpolymerization reactor or the second polymerization reactor, or both thefirst and the second polymerization reactors.

In some embodiments, the polymerization process comprises a series ofone or more continuous CSTR reactors followed by a BPL/PPL separator(such as a wiped film evaporator (WFE) or flash tank evaporatoroperating under vacuum). In other embodiments, the polymerizationprocess comprises a series of one or more loop reactors followed by aBPL/PPL separator (such as a WFE or flash tank evaporator operatingunder vacuum). In yet other embodiments, the polymerization processcomprises a series of one or more in a series of one or more CSTRreactors followed by a polishing plug flow reactor (PFR) or by a BPL/PPLseparator (Wiped Film Evaporator or flash tank evaporator operatingunder vacuum). In still other embodiments, the polymerization processcomprises a series of one or more PFR optionally followed by a BPL/PPLseparator (such as a WFE or flash tank evaporator operating undervacuum).

In some embodiments, the polymerization process comprises greater thantwo polymerization reactors. For example, in certain embodiments, thepolymerization process comprises three or more polymerization reactors,four or more polymerization reactors, five or more polymerizationreactors, six or more polymerization reactors, seven or morepolymerization reactors, or eight or more polymerization reactors. Insome variations, the reactors are arranged in series, while in othervariations, the reactors are arranged in parallel. In certainvariations, some of the reactors are arranged in series while others arearranged in parallel.

FIGS. 4A and 4B depict exemplary PPL production system/productionprocess comprising two polymerization reactors connected in series, anda PPL purification and BPL recycle system with a wiped film evaporator(WFE) for recycling of unreacted bPL back into the polymerizationreactors. With reference to FIG. 4A, the polymerization process includesbPL source 402 and polymerization catalyst source 404, configured tofeed bPL and catalyst, respectively, into reactor 408. Reactor 408includes a bPL inlet to receive bPL from the bPL source and apolymerization catalyst inlet to receive polymerization catalyst fromthe polymerization catalyst source. In some variations, the bPL inlet isconfigured to receive the bPL from the bPL source at a rate of 3100kg/hr, and the first polymerization catalyst inlet is configured toreceive the polymerization catalyst from the polymerization catalystsource at a rate of 0.1 to 5 kg/hr.

With reference again to FIG. 4A, reactor 408 further includes a mixtureoutlet to output a mixture comprising PPL, unreacted bPL, and residualcarbonylation catalyst to reactor 410. Reactor 410 is a second reactorpositioned after reactor 408, and is configured to receive the mixturefrom reactor 408 and additional polymerization catalyst frompolymerization catalyst source 406. In some variation, the mixture inletof the second reactor is configured to receive the mixture from thefirst reactor at a rate of 4500 kg/hr, and the second polymerizationcatalyst inlet is configured to receive additional polymerizationcatalyst from the catalyst source at a rate of 0.1 to 4 kg/hr.

With reference again to FIG. 4A, reactor 408 further includes a mixtureoutlet to output a mixture comprising PPL, unreacted bPL, and residualcarbonylation catalyst to evaporator 412. In some variations, themixture outlet is configured to output such mixture at a rate of 4500kg/hr.

With reference to FIG. 4B, the depicted polymerization process includesbPL source 422 and polymerization catalyst source 424, configured tofeed bPL and catalyst, respectively, into reactor 428. Reactor 428includes a bPL inlet to receive bPL from the bPL source and apolymerization catalyst inlet to receive polymerization catalyst fromthe polymerization catalyst source. In some variations, the bPL inlet isconfigured to receive the bPL from the bPL source at a rate of 3100kg/hr, and the first catalyst inlet is configured to receive thecatalyst from the catalyst source at a rate of 0.1 to 5 kg/hr.

With reference again to FIG. 4B, reactor 428 further includes a mixtureoutlet to output a mixture comprising PPL, unreacted bPL, and residualcarbonylation catalyst to reactor 430. Reactor 430 is a second reactorpositioned after reactor 428, and is configured to receive the mixturefrom reactor 428 and additional polymerization catalyst frompolymerization catalyst source 426. In some variation, the mixture inletof the second reactor is configured to receive the mixture from thefirst reactor at a rate of 4500 kg/hr, and the second polymerizationcatalyst inlet is configured to receive additional polymerizationcatalyst from the polymerization catalyst source at a rate of 0.1 to 4kg/hr.

In some variations, the mixture output from reactor 410 (FIG. 4A) andreactor 430 (FIG. 4B) is made up of at least 95% wt PPL.

Such mixture may be output from the second reactor to an evaporator.Evaporator 412 (FIG. 4A) and 432 (FIG. 4B) may be, for example, a wipedfilm evaporator, thin film evaporator, or falling film evaporator. Theevaporator is configured to produce a PPL product stream.

In some variations, the evaporator is configured to produce a PPLproduct stream having a purity of at least 98%, at least 98.5%, or atleast 99%. In other variations, the evaporator is configured to producea PPL product stream having less 0.6% wt of bPL. In some variations, thePPL stream has trace amounts of carbonylation catalyst. For example, thePPL product stream may have 0.1 mM of cobalt from the carbonylationcatalyst. In some variations, the trace amounts of carbonylationcatalyst are subsequently removed from the PPL product stream by IERbefore thermolysis, as described above in FIGS. 6, 7, 10 and 11.

In some variations, the polymerization process further includes one ormore heat exchangers. With reference to FIG. 4A, bPL from bPL source 402may be passed through heat exchanger 414 before such BPL stream is fedinto reactor 408.

It should generally be understood that the polymerization is anexothermic reaction. Thus, in other variations, reactors 408 and 410(FIG. 4A) may further include a connection to at least one heatexchanger. With reference to FIG. 4B, reactors 428 and 430 (FIG. 4B) mayfurther include a connection to at least one heat exchanger.

The reactors of polymerization process may include any suitablereactors, including, for example, continuous reactors or semi-batchreactors. In one variation, with reference to FIG. 4A, the reactors maybe continuous-flow stirred-tank reactors. The reactors may also includethe same or different stirring devices. For example, in one variation,reactor 408 may include a low velocity impeller, such as a flat blade.In other variation, reactor 410 may include a low shear mixer, such as acurved blade.

A skilled artisan would recognize that the choice for the mixing devicein each of the reactors may depend on various factors, including theviscosity of the mixture in the reactor. For example, the mixture in thefirst reactor may have a viscosity less than 1000 cP. If the viscosityis less than 1000 cP, then a low velocity impeller may be desired. Inanother example, the mixture in the second reactor may have a viscositygreater than 2000 cP. If the viscosity is greater than 2000 cP, then alow shear mixer may be desired.

In another variation, with reference to FIG. 4B, the reactors may beloop reactors.

It should be understood that while FIGS. 4A and 4B depict the use of tworeactors configured in series, other configurations are considered. Forexample, in other exemplary variations of the polymerization process,three reactors may be employed. In yet other variations where aplurality of reactors is used in the polymerization process, they may bearranged in series or in parallel.

FIG. 5 depicts an exemplary polymerization process, which includes a BPLpolymerization reactor. Polymerization reactor 500 includes mixing zone510 configured to mix the production stream entering the polymerizationprocess and catalyst, and a plurality of cooling zones 520 positionedafter the mixing zone. Polymerization reactor 500 has reaction length502, wherein up to 95% of the bPL in the entering production stream ispolymerized in the presence of the catalyst to form PPL in the first 25%of the reaction length. In some variations of the system depicted inFIG. 5, the bPL is completely converted to PPL. Such a system may beused, for example, in the complete conversion of bPL to PPL as describedabove for FIGS. 6, 8, 10 and 12.

In some variations of a polymerization reactor, the plurality of coolingzones includes at least two cooling zones. In one variation, theplurality of cooling zones includes two cooling zones or three coolingzones.

For example, polymerization reactor 500 as depicted in FIG. 5 has threecooling zones 522, 524 and 526. In one variation, the three coolingzones are connected serially in the first 25% of the reaction length. Inanother variation, cooling zone 522 is configured to receive a mixtureof bPL and the catalyst from the mixing zone at a rate of 3100 kg/hr;cooling zone 524 is configured to receive a mixture of the bPL, thecatalyst and PPL produced in cooling zone 522 at a rate of 3100 kg/hr;and cooling zone 526 is configured to receive a mixture of the bPL, thecatalyst, the PPL produced in cooling zone 522, and PPL produced incooling zone 524 at a rate of 3100 kg/hr.

In certain embodiments, the first 25% of the reaction length is a shelland a tube heat exchanger. In one variation, the shell may be configuredto circulate a heat transfer fluid to maintain a constant temperature inreaction length 502. In another variation, the tube heat exchanger isconfigured to remove heat produced in the first reaction zone.

With reference again to FIG. 5, polymerization reactor 500 furtherincludes end conversion zone 528 connected to plurality of cooling zones520. In some variations, the end conversion zone is configured toreceive a mixture of the bPL, the catalyst, and the PPL produced inplurality of cooling zones at a rate of 3100 kg/hr. In one variation,the end conversion zone has no cooling load.

In one variation, the polymerization reactor is a plug flow reactor or ashell-and-tube reactor.

The one or more polymerization reactors used in the methods describedherein may be constructed of any suitable material compatible with thepolymerization. For example, the polymerization reactor may beconstructed from stainless steel or high nickel alloys, or a combinationthereof.

In some embodiments, the polymerization process comprises a plurality ofpolymerization reactors, and the polymerization catalyst is introducedonly into the first reactor in the series. In other embodiments, thepolymerization catalyst is added separately to each of the reactors inthe series. For example, referring again to FIG. 4A, depicted is apolymerization process comprising two CSTR in series, whereinpolymerization catalyst is introduced to the first CSTR, andpolymerization catalyst is separately introduced to the second CSTR. Inother embodiments, a single plug flow reactor (PFR) is used, andpolymerization catalyst is introduced at the beginning of the reactor,while in other embodiments polymerization catalyst is introducedseparately at a plurality of locations along the length of the PFR. Inother embodiments, a plurality of PFR is used, and polymerizationcatalyst is introduced at the beginning of the first PRF. In otherembodiments, polymerization catalyst is introduced at the beginning ofeach PFR used, while in still other embodiments polymerization catalystis introduced separately at a plurality of locations along the length ofeach PFR.

The polymerization reactor may comprise any suitable mixing device tomix the polymerization reaction mixture. Suitable mixing devices mayinclude, for example, axial mixers, radial mixers, helical blades,high-shear mixers, or static mixers. Suitable mixing devices maycomprise single or multiple blades, and may be top, bottom, or sidemounted. The polymerization reactor may comprise a single mixing device,or multiple mixing devices. In some embodiments, a plurality ofpolymerization reactors is used, and each polymerization reactorcomprises the same type of mixing device. In other embodiments, eachpolymerization reactor comprises a different type of mixing device. Inyet other embodiments, some polymerization reactors comprise the samemixing device, while others comprise different mixing devices

Preferred Embodiments of Polymerization Sub-Systems

In the preferred embodiments, distillation sub-system consists of (1)one or more polymerization reactors and (2) PPL purification/BPL recyclesystem.

Preferred BPL Polymerization Reactor

Polymerization of bPL can be performed in one or more reactors operatingin series or parallel and in preferred embodiments the distillate streamconsisting of essentially pure bPL (purity greater than 99.9 wt %) withtrace amounts of low- and high-boiling impurities (non limitingimpurities are THF and Succinic Anhydride) is fed bPL Polymerizationreactor. The bPL feed stream can be fed at the temperature of the bPLpurification column overhead (50-100° C.) or can be cooled to 20-50° C.before being fed to the polymerization reactor.

The preferred combination of conditions for the polymerization of bPLinclude temperatures in the range 80-150° C., preferrably 120-145° C. atpressures below or above atmospheric in the presence of polymerizationinitiator. The preferred initiators are quaternary amine and alkalimetal salts of acrylic acid. Non limiting examples of polymerizationinitiators are Sodium Acrylate, Potassium Acrylate, TetrabutylammoniumAcrylate. The molar ratio of polymerization initiator to bPL is from1:20000 to 1:100, preferably from 1:15000 to 1:500, preferably from1:10000 to 1:1000, and most preferably from 1:8000 to 1:1500.

In such preferred embodiments, solid polymerization initiator is mixedwith fresh bPL stream before the reactor; a high shear mixer can be usedto achieve good mixing of bPL with initiator. In another embodiment,solid polymerization initiator is mixed with recycled bPL stream beforethe reactor; a high shear mixer can be used to achieve good mixing ofbPL with initiator. In another embodiment, polymerization reactor if feddirectly into the polymerization reactor; optionally, an educator can beused to effectively mix solid initiator with all or part of bPL feed atthe inlet to the reactor.

During polymerization of bPL to form PPL Acrylic Acid that acts as chaintransfer agent can be formed in-situ. In some embodiments small amountsof acrylic acid can be fed to polymerization reactor to controlmolecular weight of PPL. To avoid radical polymerization of acrylicacid, radical polymerization inhibitors such as phenothiazine (PTZ) canbe fed to the polymerization reactor. The concentration of radicalpolymerization inhibitor in the reactor is maintained at 50-500 ppm (byweight); preferred inhibitor concentration is in the range from 150 to250 ppm.

If the plurality of polymerization reactors are operating in series, bPLcan be fed to the first reactor only or bPL feed can be split betweenreactors in series. If the plurality of polymerization reactors areoperating in series, a polymerization initiator can be fed to the firstreactor only or initiator can be fed to each of the reactors in series.

In one of the preferred embodiments, polymerization of bPL can beconducted in one or more Continuous Stirred Tank Reactors (CSTR)operating in series. The polymerization reaction is exothermic and heatof the reaction can be removed by means known in the art such as aninternal heat exchanger or jacket, an external heat exchanger (reactionmixture is circulated through external heat exchanger and cooled streamis returned to the reactor), evaporative cooling (reactor is equippedwith attached condenser: bPL is evaporated from the reactor, condensedin the condenser, and cooled bPL stream is returned to the reactor). Thereactors can be operated at atmospheric pressure, below atmosphericpressure, above atmospheric pressure.

In another preferred embodiment, polymerization of bPL can be conductedin one or more Loop Reactors operating in series. The reactors can beoperated at or above atmospheric pressure. The temperatures of thesurfaces in contact with the reaction mixture containing bPL and PPL arekept at temperatures that prevent precipitation of PPL (PPL meltingpoint is at about 70-80° C.)

In another preferred embodiment, polymerization of bPL is conducted inthe reactor system consisting of one or more CSTR or Loop Reactorsfollowed by one or more Plug Flow Reactors (PFR). The temperatures ofthe surfaces in contact with the reaction mixture containing bPL and PPLare kept at temperatures that prevent precipitation of PPL (PPL meltingpoint is at about 70-80° C.)

The concentration of PPL in the stream exiting the reaction system (bPLconversion) is greater than 40 wt %, preferably greater than 60 wt %,preferably greater than 75 wt %. The conversion of bPL can be greaterthan 80%, greater than 90%, greater than 95%, or greater than 99%. Thestream exiting bPL polymerization system is fed forward to PPLpurification and bPL recycle system. In one embodiment, polymerizationreactor product stream consists of about 80 wt % PPL, about 20 wt % bPL,and polymerization initiator incorporated into PPL molecules.

Preferred PPL Purification/BPL Recycle System

The polymerization reactor product consisting of PPL product andunreacted bPL is fed forward to PPL purification and bPL recycle system.In preferred embodiments bPL can be separated from PPL in one or moreflash evaporators operating under vacuum, or one or more Wiped FilmEvaporators (WFE) operating under vacuum, or a combination thereof. Toavoid decomposition of bPL within this system, surface temperatures incontact with bPL are kept below 200° C., preferably below 180° C., mostpreferably below 160° C. Recovered bPL is fed back to the polymerizationreactor. Purified PPL contains less than 0.5 wt % bPL, preferably lessthan 0.25 wt % bPL, preferably less than 0.1 wt % bPL, and preferablyconcentration of bPL in PPL product is less than 100 ppm. Mostpreferably PPL is fed forward to thermolysis reaction system forproduction of Acrylic Acid or pelletized for storage or shipment.

BPL Conversion

In some variations, between 5% and 100%, between 10% and 100%, between20% and 100%, between 30% and 100%, between 40% and 100%, between 50%and 100%, between 60% and 100%, between 70% and 100%, between 80% and100%, between 90% and 100, or between 95% and 100% of the bPL isconverted to PPL in the polymerization process.

In some variations, bPL is partially converted to PPL in thepolymerization process. For example, in some variations, completeconversion of bPL to PPL is greater than or equal to 75%, and partialconversion of bPL to PPL is less than 75%. In other variations, completeconversion of bPL to PPL is greater than or equal to 80%, and partialconversion of bPL to PPL is less than 80%. In other variations, completeconversion of bPL to PPL is greater than or equal to 85%, and partialconversion of bPL to PPL is less than 85%. In yet other variations,complete conversion of bPL to PPL is greater than or equal to 90%, andpartial conversion of bPL to PPL is less than 90%. In yet othervariations, complete conversion of bPL to PPL is greater than or equalto 95%, and partial conversion of bPL to PPL is less than 95%. In onevariation, complete conversion of bPL to PPL is greater than or equal to99%, and partial conversion of bPL to PPL is less than 99%.

In other variations, partial conversion is between 30% and 90%; between40% and 90%, between 50% and 90%; or between 60% and 90%.

In some variations, the polymerization process comprises a plurality ofpolymerization reactors, and the conversion of bPL to PPL in eachreactor is between 5% and 100%, between 10% and 100%, between 20% and100%, between 30% and 100%, between 40% and 100%, between 50% and 100%,between 60% and 100%, between 70% and 100%, between 80% and 100%,between 90% and 100, or between 95% and 100% of the bPL is converted toPPL.

In some variations, the polymerization process comprises a plurality ofpolymerization reactors, and the conversion of bPL to PPL over theentire polymerization process is between 5% and 100%, between 10% and100%, between 20% and 100%, between 30% and 100%, between 40% and 100%,between 50% and 100%, between 60% and 100%, between 70% and 100%,between 80% and 100%, between 90% and 100, or between 95% and 100% ofthe bPL is converted to PPL.

In one variation, two reactors are operated in series, and theconversion of bPL to PPL in each reactor is between 10% and 100%.

As described above in FIGS. 9-13, in some embodiments of the methods toproduce PPL as described herein, the bPL is completely converted to PPL.In other embodiments, the bPL is partially converted to PPL.

BPL Conversion

Without wishing to be bound by any theory, the polymerization of bPL toPPL proceeds quickly when the concentration of reactants is high and theconcentration of products is low. As the reaction progresses to producemore products, the driving force for conversion is reduced. Thisphenomenon leads reactors which perform full conversion to be largerthan those that perform partial conversion. Thus, in certainembodiments, the polymerization conditions and reactor size are selectedsuch that conversion of bPL to PPL is partial (for example, 70%conversion), and a bPL/PPL separation device (for example, a WFE ordistillation column) is used to recycle reactants back to the inlet ofthe reactor. Without wishing to be bound by any theory, this may avoidthe requirements of a relatively large reactor while still generating arelatively pure product. In addition, the unreacted bPL is removed,which may make the handling of PPL easier. In the case where no PPL isisolated, removal of bPL reduces the possibility of other productsforming during the thermolysis reaction.

PPL Product Stream

In some embodiments, the production system/production process canproduce at least about 2000 kg/hr PPL, at least about 2500 kg/hr PPL, atleast about 3000 kg/hr PPL, at least about 3050 kg/hr PPL, or at leastabout 3500 kg/hr PPL, at least about 3638 kg/hr PPL, at least about 4000kg/hr PPL, at least about 5000 kg/hr PPL, at least about 1000 kg/hr PPL,at least about 20000 kg/hr PPL, or at least about 35000 kg/hr PPL. Insome embodiments, the production system/production process can produceabout 2000 kg/hr PPL, about 2500 kg/hr PPL, about 3000 kg/hr PPL, about3500 kg/hr PPL, about 3638 kg/hr PPL, about 4000 kg/hr PPL, about 5000kg/hr PPL, about 1000 kg/hr PPL, about 20000 kg/hr PPL, or about 35000kg/hr PPL. In some embodiments, the production system/production processcan produce between 2000 kg/hr PPL and 3500 kg/hr PPL, between 2500kg/hr PPL and 3500 kg/hr PPL, between bout 3000 kg/hr PPL and 3500 kg/hrPPL, between 2000 kg/hr PPL and 35000 kg/hr PPL, between 2500 kg/hr PPLand 35000 kg/hr PPL, between 3000 kg/hr PPL and 35000 kg/hr PPL, between3500 kg/hr PPL and 35000 kg/hr PPL, between 3638 kg/hr PPL and 35000kg/hr PPL, between 4000 kg/hr PPL and 35000 kg/hr PPL, between 5000kg/hr PPL and 35000 kg/hr PPL, between 1000 kg/hr PPL and 35000 kg/hrPPL, or between 20000 kg/PPL and 35000 kg/hr PPL.

In some embodiments, the production system/production process canproduce at least about 25 kmol/hr PPL, at least about 30 kmol/hr PPL, atleast about 40 kmol/hr PPL, at least about 42 kmol/hr PPL, or at leastabout 50 kmol/hr PPL. In some embodiments, the mass fraction of PPL inthe PPL product stream in the production system/production process afterpolymerization can be at least about 0.90, at least about at least about0.95, at least about 0.98, at least about 0.982, and at least about0.99. In some embodiments, the mole fraction of PPL in the PPL productstream of the production system/production process after polymerizationcan be at least about 0.90, at least about at least about 0.95, at leastabout 0.98, at least about 0.984, and at least about 0.99. The remainderof the PPL product stream can include unreacted bPL (in mole fraction ofat most about 0.02, at most about 0.015, or at most about 0.011),secondary reaction products such as succinic anhydride (in mole fractionof at most about 0.01, at most about 0.005, or at most about 0.004) andleft over solvent (e.g., THF) and leftover carbonylation catalyst orcomponents thereof (in at most about 1000 ppm). The PPL product streamcan then receive thermolysis processing to form GAA. In someembodiments, the PPL product stream of the production system/productionprocess can have a temperature between about 50-150° C., between about110-150° C., or about 145° C. In some embodiments, the PPL productstream of the production system/production process can be at a pressureof at least about 0.001 bar, about 0.001-1 bar, or at least about 0.005bar.

In certain embodiments, a method is provided for the production (e.g.,integrated production) of a composition comprising PPL chains of Formula(B):

where n is an integer from 10 to about 1,000 and Y is either —H or acation,comprising the step of polymerizing bPL in the presence of a chaintransfer agent selected from the group consisting of: a compound ofFormula (C):

or a salt thereof, or a mixture of any two or more of these, where p isfrom 0 to 9. In certain embodiments, the composition further comprisesPPL.

In certain embodiments, the PPL composition formed is characterized inthat at least 90%, 95%, 99%, 99.5%, 99.8 or 99.9% of the polymer chainsin the composition have an acrylate end group.

In certain embodiments, the PPL composition formed is characterized inthat at least 90%, 95%, 99%, 99.5%, 99.8 or 99.9% of the polymer chainsin the composition are of Formula (B).

In certain embodiments, n is, on average in the polypropiolactonecomposition, between 10 and 50, or between 50 and 100, or between 100and 150, or between 150 and 250, or between 250 and 350, or between 350and 500.

In some embodiments, the system described herein is configured toproduce polypropiolactone with an average molecular weight between 800g/mol and 100000 g/mol, between 500 g/mol and 70000 g/mol, between 1000g/mol and 60000 g/mol, or between 1500 g/mol and 40000 g/mol. In someembodiments, the molecular weight is number average molecular weight,while in other embodiments, the molecular weight is weight averagemolecular weight.

In certain embodiments, the PPL composition is characterized in that ithas a polydispersity index (PDI) of less than 10.

In certain embodiments, the PPL composition is characterized in that ithas a PDI less than 8, or less than 5, or less than 3, or less than 2.5,or less than 2.0.

Cobalt/Ion Removal from PPL

In some embodiments, the PPL product stream is treated to reduce theconcentration of cobalt and/or ions. The cobalt may be a cobalt ion oruncharged cobalt, or a combination thereof. The ions may be cobalt ionsor non-cobalt ions.

In certain variations, the cobalt is a cobalt ion. The cobalt may befrom decomposition of the carbonylation catalyst, residual catalystcomponents which comprise cobalt, or residual catalyst, or combinationsthereof. For example, in some embodiments, the carbonylation catalystdecomposes to produce Co⁻¹, Co, Co⁺, Co²⁺, or Co³⁺, or combinationsthereof. Thus, in some embodiments, the cobalt is a cobalt ion, while inother embodiments the cobalt is not a cobalt ion.

In some variations, at least some ions are removed from the PPL productstream. In some variations, the ions comprise metal ions. In otherembodiments, the ions comprise non-metal ions. In yet other embodiments,the ions comprise both metal and non-metal ions. As discussed above, incertain variations, the ions comprise cobalt ions. The ions may be fromdecomposition of the carbonylation catalyst, residual catalystcomponents which comprise ions, residual catalyst, or ions produced asbyproducts of the carbonylation reaction, or combinations thereof. Forexample in some embodiments, the carbonylation catalyst decomposes toproduce Co⁻¹, Co⁺, Co²⁺, Co³⁺, or Al³⁺, or combinations thereof. Inother embodiments, ions produced as byproducts of the carbonylationreaction include acetate (CH₃C(O)O⁻) or acrylate (CH₂═CHC(O)O⁻), or acombination thereof.

In certain embodiments, the step of treating the PPL product stream toremove at least a portion of cobalt and/or ions comprises ion exchangeof cobalt and/or ions using ion exchange materials. In some embodiments,it may be possible to use an ion exchange resing for the ion exchangematerial. The ion exchange materials may be cationic, anionic,amphoteric, Lewis basic, Lewis acidic, or may comprise chelating groups.In certain embodiments, the ion exchange material may be a cationexchanger. In certain embodiments, functional groups on the cationexchange materials may be selected from: —SO₃, PO₃ ²⁻, —COOH, —C₆H₄OH,—SH, —AsO₃, or —SeO₃, or combinations of two or more of these. Incertain embodiments, functional groups on the cation exchange materialscomprise —SO₃.

In certain embodiments, the ion exchange material may be an anionexchanger. In certain embodiments, functional groups on the anionexchange materials may be selected from: —N⁺(alkyl)₃, —N⁺(CH₃)₃,—N⁺(CH₃)₂C₂H₄OH, —N⁺(CH₃)₂C₂H₅, —P⁺(alkyl)₃, —P⁺(aryl)₃, —P⁺(C₄H₃)₃, or—^(P)+(Ph)₃, or combinations of two or more of these. In certainembodiments, functional groups on the anion exchange materials comprise—N⁺(alkyl)₃. In certain embodiments, functional groups on the anionexchange materials comprise —P⁺(alkyl)₃. In certain embodiments,functional groups on the anion exchange materials comprise —P⁺(aryl)₃.

In certain embodiments where the step of treating the PPL product streamto separate cobalt and/or ions comprises ion exchange, the processentails both anion exchange and cation exchange. In certain embodimentsthe anion and cation exchange are performed concomitantly. In certainembodiments, the anion and cation exchange are performed sequentially.In certain embodiments, the anion exchange is performed first followedby cation exchange. In certain embodiments, the cation exchange isperformed first followed by anion exchange. In certain embodiments, anorganic ion exchange resin may prove useful in the separation stepcomprises an organic ion exchange resin. The general characteristics andproperties of such resins are the same as previously described.

In various aspects, the bead size may be widely distributed, or may bevery narrow, so-called mono-disperse resins. In embodiments wherecatalyst is removed from the PPL product stream by ion exchange, the ionexchange material can be contacted with the PPL product stream by anyconventional method. This includes, but is not limited to: flowing thePPL product stream through a fixed bed of a solid ion exchange material(i.e. in the form of beads, granules or other particles); flowing thePPL product stream through a fluidized bed of adsorbent, flowing the PPLproduct stream through fabrics, meshes, or filtration plates comprisingthe ion exchange material, or slurrying the PPL product stream with theion exchange material (typically followed by filtration, centrifugation,sedimentation or the like to remove the ion exchange material from thePPL product stream). In embodiments where the PPL product stream isflowed through a packed column of ion exchange material, it may bedesirable to provide a plurality of such columns in parallel with aprovision to switch the flow from one to another periodically. Thus whenone column of ion exchange material becomes saturated with cobalt and/orions removed from the PPL product stream, it can be switched out of theflow path and the flow diverted to a fresh column—in certainembodiments, the interval of time from when a column is placed in theflow path to when it is switched out of the flow path corresponds to the“first time interval” recited in the methods described herein.

Where an ion exchange material is used to remove cobalt and/or ions fromthe PPL product stream, the inventive methods may include a subsequentstep of removing the cobalt and/or ions from the ion exchange material.Such removal methods are well known in the art and typically involvecontacting the ion exchange resin with a strong solution of a salt, theanion or cation of which will displace the adsorbed component from theion exchange material.

In certain variations, the cobalt is Co⁻¹, Co, Co⁺, Co²⁺, or Co³⁺, or acombination thereof. In some embodiments, the PPL product stream priorto cobalt removal has a cobalt concentration between 0.001 mM and 5 mM,between 0.01 mM and 3 mM, between 0.01 mM and 2 mM, between 0.01 mM and1 mM, between 0.05 mM and 0.5 mM, between 0.05 mM and 0.2 mM, or between0.07 mM and 0.15 mM. In some embodiments, the cobalt concentration ofthe permeate prior to cobalt removal is about 0.01 mM, about 0.03 mM,about 0.06 mM, about 0.09 mM, about 0.1 mM, about 0.13 mM, about 0.16mM, about 0.19 mM, about 0.2 mM, about 0.23 mM, about 0.26 mM, about0.29 mM, or about 0.3 mM. In one embodiment, the cobalt concentration ofthe PPL before cobalt removal is about 0.1 mM.

Thus, in some embodiments, the concentration of cobalt in the PPLproduct stream before contacting the ion exchange resin is between 0.001mM and 5 mM, between 0.01 mM and 3 mM, between 0.01 mM and 2 mM, between0.01 mM and 1 mM, between 0.05 mM and 0.5 mM, between 0.05 mM and 0.2mM, or between 0.07 mM and 0.15 mM.

In some embodiments, the concentration of cobalt in the PPL productstream after contacting the ion exchange resin is between 0.001 mM and 1mM, 0.001 mM and 0.5 mM, between 0.001 mM and 0.05 mM, between 0.005 mMand 0.02 mM, or between 0.007 mM and 0.015 mM. In one variation, theconcentration of cobalt in the PPL product stream after contacting theion exchange resin is 0.01 mM.

In some embodiments, at least some aluminum is removed from the PPLproduct stream. In certain variations, the aluminum is Al³⁺. In someembodiments, the PPL product stream prior to aluminum removal has analuminum concentration between 0.001 mM and 5 mM, between 0.01 mM and 3mM, between 0.01 mM and 2 mM, between 0.01 mM and 1 mM, between 0.05 mMand 0.5 mM, or between 0.09 mM and 0.2 mM. In some embodiments, the PPLproduct stream prior to aluminum removal has a aluminum concentration ofabout 0.01 mM, about 0.03 mM, about 0.06 mM, about 0.09 mM, about 0.1mM, about 0.13 mM, about 0.16 mM, about 0.19 mM, about 0.2 mM, about0.23 mM, about 0.26 mM, about 0.29 mM, or about 0.3 mM. In oneembodiment, the aluminum concentration of the PPL product stream beforealuminum removal is about 0.1 mM.

Thus, in some embodiments, the concentration of aluminum in the PPLproduct stream before contacting the ion exchange resin is between 0.001mM and 5 mM, between 0.01 mM and 3 mM, between 0.01 mM and 2 mM, between0.01 mM and 1 mM, between 0.05 mM and 0.5 mM, between 0.05 mM and 0.2mM, or between 0.07 mM and 0.15 mM.

In some embodiments, the concentration of aluminum in the PPL productstream after contacting the ion exchange resin is between 0.001 mM and 1mM, 0.001 mM and 0.5 mM, between 0.001 mM and 0.05 mM, between 0.005 mMand 0.02 mM, or between 0.007 mM and 0.015 mM. In one variation, theconcentration of aluminum in the PPL product stream after contacting theion exchange resin is 0.01 mM.

Solid PPL

In some embodiments, the production system/production process describedherein further comprises a PPL stream processing system configured toreceive the PPL product stream and produce solid PPL. For example, inone embodiment, the PPL product stream is fed into at least one inlet ofa PPL stream processing system, and solid PPL exits at least one outletof the PPL stream processing system. The PPL stream processing systemmay be configured to produce solid PPL in any suitable form. Forexample, in some embodiments, the PPL stream processing system isconfigured to produce solid PPL in pelleted form, flaked form,granulated form, or extruded form, or any combinations thereof. Thus,solid PPL flakes, solid PPL pellets, solid PPL granules, or solid PPLextrudate, or any combinations thereof, may exit the outlet of the PPLstream processing system. The PPL stream processing system may includeone or more flaking devices, pelleting devices, extrusion devices, orgranulation devices, or any combinations thereof.

Geographic Location

In certain embodiments, the production system/production processdescribed herein produces a PPL product stream at a first location, thePPL product stream is processed to produce solid PPL, and the solid PPLis converted to a GAA product stream in a second location. In someembodiments, the first location and the second location are at least 100miles apart. In certain embodiments, the first location and the secondlocation are between 100 and 12,000 miles apart. In certain embodiments,the first location and the second location are at least 250 miles, atleast 500 miles, at least 1,000 miles, at least 2,000 or at least 3,000miles apart. In certain embodiments, the first location and the secondlocation are between about 250 and about 1,000 miles apart, betweenabout 500 and about 2,000 miles apart, between about 2,000 and about5,000 miles apart, or between about 5,000 and about 10,000 miles apart.In certain embodiments, the first location and the second location arein different countries. In certain embodiments, the first location andthe second location are on different continents.

In certain embodiments, the solid PPL is transported from the firstlocation to the second location. In some embodiments, the solid PPL istransported a distance of more than 100 miles, more than 500 miles, morethan 1,000 miles, more than 2,000 miles or more than 5,000 miles. Incertain embodiments, the solid PPL is transported a distance of between100 and 12,000 miles, between about 250 and about 1000 miles, betweenabout 500 and about 2,000 miles, between about 2,000 and about 5,000miles, or between about 5,000 and about 10,000 miles. In someembodiments, the solid PPL is transported from a first country to asecond country. In certain embodiments, the solid PPL is transportedfrom a first continent to a second continent.

In certain embodiments, the solid PPL is transported from the NorthAmerica to Europe. In certain embodiments, the solid PPL is transportedfrom the North America to Asia. In certain embodiments, the solid PPL istransported from the US to Europe. In certain embodiments, the solid PPLis transported from the US to Asia. In certain embodiments, the solidPPL is transported from the Middle East to Asia. In certain embodiments,the solid PPL is transported from the Middle East to Europe. The solidPPL may be transported by any suitable means, including, for example, bytruck, train, tanker, barge, or ship, or any combinations of these. Insome embodiments, the solid PPL is transported by at least two methodsselected from truck, train, tanker, barge, and ship. In otherembodiments, the solid PPL is transported by at least three methodsselected from truck, train, tanker, barge, and ship.

In some embodiments, the solid PPL is in the form of pellets, flakes,granules, or extrudate, or any combination thereof. In some variations,the solid PPL is converted to a GAA product stream using the thermolysisreactor as described herein. In some variations, the solid PPL is fedinto an inlet of the thermolysis reactor and is converted to a GAAproduct stream. In other embodiments, the solid PPL is converted tomolten PPL, and the molten PPL is fed into an inlet of the thermolysisreactor as described herein and converted to a GAA product stream.

Acrylic Acid Production System/Production Process

Polypropiolactone (PPL) can generally be converted to acrylic acid (AA)according to the following scheme:

In certain embodiments, the polypropiolactone produced undergoesthermolysis continuously (e.g. in a fed batch reactor or othercontinuous flow reactor format). In certain embodiments, the continuousthermolysis process is linked to a continuous polymerization process toprovide acrylic acid at a rate matched to the consumption rate of thereactor.

Thermolysis Reactors

In some embodiments, the thermolysis reactor is a fluidized bed reactor.Inert gas may be used to fluidize inert solid heat transfer medium(HTM), and polypropiolactone is fed to the reactor. In some variations,the polypropiolactone may be fed to the reactor in molten form, forexample, via a spay nozzle. The molten form may help facilitate thedispersion of polypropiolactone inside the reactor.

The reactor may be equipped with a cyclone that returns HTM solid backto the reactor. The inert gas, glacial acrylic acid, and higher boilingimpurities (such as succinic anhydride and acrylic acid dimer) are fedfrom the cyclone to a partial condenser where impurities are separated.For example, the condenser may be used to condense the high boilingimpurities, and such impurities can then be purged from the reactor as aresidual waste stream.

Glacial acrylic acid with the inert gas may be fed to a second condenserwhere the glacial acrylic acid and the inert gas are separated. A liquidglacial acrylic acid stream is output from the second condenser, and theinert gas is output as a separate stream that may be returned back tothe reactor to fluidize the heat transfer solid. The glacial acrylicacid stream may be used for condensation/absorption and then storage.

The residual waste stream purged from the reactor may include, forexample, high boiling organics (or organic heavies), for example,resulting from the polymerization catalyst and succinic anhydride, aswell as the cationic and anionic carbonylation catalyst species ifcarbonylation catalyst was not separated prior to the thermolysisreactor. In some embodiments, the high boiling organics (or organicheavies) may include any compounds which are not acrylic acid. Incertain embodiments, the high boiling organics (or organic heavies) mayinclude any compounds which remain in the bottoms stream aftercondensing the acrylic acid in the glacial acrylic acid productionsystem/production process. In some embodiments, the high boilingorganics (or organic heavies) may include succinic anhydride,polymerization catalyst, or carbonylation catalyst or components thereof(for example, organic compounds from the carbonylation catalyst). Insome embodiments, the high boiling organics (or organic heavies) have aboiling point higher than acrylic acid.

In other embodiments, the thermolysis reactor is a moving bed reactor.Polypropiolactone is fed into a moving bed reactor as a solid andglacial acrylic acid exits the reactor as a vapor stream and is thencondensed.

Conditions

In some variations, the operating temperature in the thermolysis reactoris from about 150° C. to about 300° C., from about 150° C. to about 200°C., from about 150° C. to about 250° C., from about 175° C. to about300° C., from about 200° C. to about 250° C., from about 225° C. toabout 275° C., from about 250° C. to about 300° C., from about 200° C.to about 300° C., from about 200° C. to about 400° C., or from about200° C. to about 500° C. In some variations, operating temperature isthe average temperature of the contents of the reactor.

In some variations, the operating pressure in the thermolysis reactor isfrom about 0.01 atmospheres to about 500 atmospheres (absolute), fromabout 0.01 atmospheres to about 10 atmospheres (absolute), from about0.01 atmospheres to about 50 atmospheres (absolute), from about 1atmosphere to about 10 atmospheres (absolute), from about 1 atmosphereto about 50 atmospheres (absolute), from about 1 atmosphere to about 100atmospheres (absolute), from about 10 atmospheres to about 50atmospheres (absolute), from about 10 atmospheres to about 100atmospheres (absolute), from about 50 atmospheres to about 100atmospheres (absolute), from about 50 atmospheres to about 200atmospheres (absolute), from about 100 atmospheres to about 200atmospheres (absolute), from about 100 atmospheres to about 250atmospheres (absolute), from about 200 atmospheres to about 300atmospheres (absolute), from about 200 atmospheres to about 500atmospheres (absolute), or from about 250 atmospheres to about 500atmospheres (absolute).

In a particularly preferred embodiment the PPL stream from a bPLpolymerization system enters primary thermolysis reactor, either insolid or liquid phase at a temperature between 100° C. and 320° C., andabsolute pressure between 1 mmHg and 5000 mmHg. One of many methods mayprovide heat transfer input, for example internal coils, external heatexchanger with a pump-around loop from and back to the primary reactor,or a baffled jacket on the walls of the reactor. Alternatively, a hightemperature liquid or gas that that does not significantly affect thereaction chemistry may be introduced to maintain desired reactiontemperature and separated downstream. Depending upon time andtemperature residence time for complete conversion may vary from a fewseconds to 24 hours or more. Mixing of the contents of the reactor mayalso improve mass and heat transfer.

Preferably the thermolysis conditions and arrangement will minimize theloss of PPL. to polyacrylic acid. Representative ways of avoidingpolyacrylic acid production include the use of a depolymerizationcatalyst to decrease required reaction severity to decrease the reactionrate of acrylic acid to polyacrylic acid relative to PPL to acrylicacid; the use of high concentrations of radical polymerizationinhibitor; and/or means to minimize the concentration of acrylic acid inthe liquid phase.

A continuous PPL thermolysis design (continuous, equal mass flows in andout of the primary reactor) can minimize the concentration of acrylicacid in the liquid phase, which lowers the reaction rate of acrylic acidto polyacrylic acid relative to that of PPL to acrylic acid. Removingvapors from the headspace of the primary reactor will lower the acrylicacid partial pressure in the headspace of the reactor and its liquidcontents. Sparging with an inert gas, preferably continuously willfurther reduce the concentration of acrylic acid in the reactor's liquidcontents. Withdrawal of liquid effluent stream and any other nonvolatilecomponents may also be desired to manage accumulation of polyacrylicacid. These may be directed to a second thermolysis reactor, to wastetreatment, or to a reactive distillation to convert the considerable PPLin the stream to volatile species such as acrylic acid and short-chainPPL oligomers. The vapor effluent from this distillation operation canflow back to the primary reactor, or be mixed with the vapor effluentfrom the primary reactor.

The vapor effluent from the various forms and number of suitablethermolysis reactor preferably, before going to product storage,undergoes condensation; passes in vapor phase to a distillationoperation to remove higher-boiling and/or lower-boiling impuritiesbefore condensation; goes to condensation, then to a distillation inliquid phase to remove higher-boiling and/or lower-boiling impuritiesand then condensation. In another embodiment the vapor effluent iscondensed internally and isolated from the products that arenon-volatile before undergoing further purification via distillationbefore storage or goes directly to product storage. Limiting thetemperature of any liquid-phase acrylic acid is known to limit yields topolyacrylic acid. Preferably radical polymerization inhibitor shall beuse in all liquid phase acrylic acid. The bottoms from a distillationoperation shall optimally be returned to the primary thermolysis reactorfor further thermolysis, but may be disposed of as well.

In some variations, the thermolysis process is operated under an oxygenand water free atmosphere. For example, in certain variations, theamount of oxygen present in the thermolysis reactor is less than 1 wt %,less than 0.5 wt %, less than 0.01 wt %, or less than 0.001 wt %. Incertain variations, the amount of water present in the thermolysisreactor is less than 1 wt %, less than 0.5 wt %, less than 0.01 wt %, orless than 0.001 wt %.

Glacial Acrylic Acid

In some variations, glacial acrylic acid produced according to thesystems and methods described herein has a purity of at least 98%, atleast 98.5%, at least 99%, at least 99.1%, at least 99.2%, at least99.3%, at least 99.4%, at least 99.5%, at least 99.6%, at least 99.7%,at least 99.8%, or at least 99.9%; or between 99% and 99.95%, between99.5% and 99.95%, between 99.6% and 99.95%, between 99.7% and 99.95%, orbetween 99.8% and 99.95%.

In other variations, acrylic acid produced according to the systems andmethods described herein is suitable to make high molecular weightpolyacrylic acid. In certain variations, acrylic acid produced accordingto the systems and methods described herein may have a lower purity,such as 95%. Thus, in one variation, the acrylic acid has a purity of atleast 95%.

In yet other variations, the glacial acrylic acid has:

(i) a cobalt level of less than 10 ppm, less than 100 ppm, less than 500ppm, less than 1 ppb, less than 10 ppb, or less than 100 ppb; or

(ii) an aluminum level of less than 10 ppm, less than 100 ppm, less than500 ppm, less than 1 ppb, less than 10 ppb, or less than 100 ppb; or

(iii) a β-propiolactone level of less than 1 ppm, less than 10 ppm, lessthan 100 ppm, less than 500 ppm, less than 1 ppb, or less than 10 ppb;

(iv) an acrylic acid dimer level of less than 2000 ppm, less than 2500ppm, or less than 5000 ppm; or

(v) a water content of less than 10 ppm, less than 20 ppm, less than 50ppm, or less than 100 ppm,

or any combination of (i) to (v).

Unlike known methods to produce glacial acrylic acid, acetic acid,furfurals and other furans are not produced and thus, are not present inthe glacial acrylic acid produced.

Glacial acrylic acid may be used to make polyacrylic acid forsuperabsorbent polymers (SAPs) in disposable diapers, training pants,adult incontinence undergarments and sanitary napkins. The low levels ofimpurities present in the glacial acrylic acid produced according to thesystems and methods herein help to facilitate a high-degree ofpolymerization to acrylic acid polymers (PAA) and avoid adverse effectsfrom by-products in end applications. For example, aldehyde impuritiesin acrylic acid hinder polymerization and may discolor the polymerizedacrylic acid. Maleic anhydride impurities form undesirable copolymerswhich may be detrimental to polymer properties. Carboxylic acids, e.g.,saturated carboxylic acids that do not participate in thepolymerization, can affect the final odor of PAA or SAP-containingproducts and/or detract from their use. For example, foul odors mayemanate from SAP that contains acetic acid or propionic acid and skinirritation may result from SAP that contains formic acid. The reductionor removal of impurities from petroleum-based acrylic acid is costly,whether to produce petroleum-based crude acrylic acid or petroleum-basedglacial acrylic acid. Such costly multistage distillations and/orextraction and/or crystallizations steps are generally employed (e.g.,as described in U.S. Pat. Nos. 5,705,688 and 6,541,665).

GAA Production System/Production Process

In some embodiments, the production system/production process canproduce at least about 25 kilo tons per annum (“KTA”) glacial acrylicacid (“GAA”), at least about 160 KTA GAA, at least about 250 KTA GAA, orat least about 400 KTA GAA for annual production operation of about 8000hours. In some embodiments, the production system/production process canproduce at least about 2000 kg/hr GAA, at least about 2500 kg/hr GAA, atleast about 3000 kg/hr GAA, at least about 3025 kg/hr GAA, at leastabout 3500 kg/hr GAA, at least about 3638 kg/hr GAA, at least about 4000kg/hr GAA, at least about 5000 kg/hr GAA, at least about 1000 kg/hr GAA,at least about 20000 kg/hr GAA, or at least about 35000 kg/hr GAA. Insome embodiments, the production system/production process can produceabout 2000 kg/hr GAA, about 2500 kg/hr PPL, about 3000 kg/hr GAA, about3500 kg/hr GAA, about 3638 kg/hr GAA, about 4000 kg/hr GAA, about 5000kg/hr GAA, about 1000 kg/hr GAA, about 20000 kg/hr GAA, or about 35000kg/hr GAA. In some embodiments, the production system/production processcan produce between 2000 kg/hr GAA and 3500 kg/hr GAA, between 2500kg/hr GAA and 3500 kg/hr GAA, between bout 3000 kg/hr GAA and 3500 kg/hrGAA, between 2000 kg/hr GAA and 35000 kg/hr GAA, between 2500 kg/hr GAAand 35000 kg/hr GAA, between 3000 kg/hr GAA and 35000 kg/hr GAA, between3500 kg/hr GAA and 35000 kg/hr GAA, between 3638 kg/hr GAA and 35000kg/hr GAA, between 4000 kg/hr GAA and 35000 kg/hr GAA, between 5000kg/hr GAA and 35000 kg/hr GAA, between 1000 kg/hr GAA and 35000 kg/hrGAA, or between 20000 kg/hr GAA and 35000 kg/hr GAA. In someembodiments, the production system/production process can produce atleast about 25 kmol/hr GAA, at least about 30 kmol/hr GAA, at leastabout 35 kmol/hr GAA, at least about 40 kmol/hr GAA, at least about 42kmol/hr, or at least about 50 kmol/hr GAA. The remainder of the GAAproduct stream can include secondary reaction products such as succinicanhydride and left over solvent such as THF. In some embodiments, theGAA product stream of the production system/production process can havea temperature between about 20-60° C., between about 30-50° C., or about40° C. In some embodiments, the GAA product stream of the productionsystem/production process can be at a pressure of at least about 0.5bar, about 0.5-1.5 bar, or at least about 1 bar.

POLYMERIZATION EXAMPLES Example 1

Batch bPL Polymerization Using Sodium Acrylate as Initiator

Under nitrogen, a Parr reactor equipped with an ATR-IR sentinel wascharged with 16.2 mg of sodium acrylate. The reactor was sealed andheated to 100° C. In a 50 mL stainless vessel, a mixture of 11.8 mg ofphenothiazine and 25 g of beta-propiolactone was added under nitrogen.The vessel was sealed and connected to the reactor. The mixture ofbeta-propiolactone and phenothiazine was injected into the reactorcontaining sodium acrylate with 50 psi of CO pressure at 100° C. Thereaction was agitated to 500 rpm, and monitored by in-line IR. The plotof beta-propionate peak at 1836 cm-1 and poly(propiolactone) peak at1739 cm-1 as a function of time is shown in FIG. 17. After thetemperature was stabilized, the reaction temperature was set to 145° C.And the reaction was run for 5 hours, by which time, the reaction wentto completion.

The polymer formed in the reactor was extracted with CHCl3. Volatileswere stripped off by a rotovap. The polymer was further dried under ahigh vacuum to yield 21.8 g of a white solid. The solid was analyzed by1H NMR, TGA, SEC, and melt rheology. SEC of the isolated solid gave amMn of 3710 and an Mw of 8740.

Example 2

Batch bPL Polymerization Using Tetra(Butylammonium) Acrylate asInitiator

Under nitrogen, a Parr reactor equipped with an ATR-IR sentinel wascharged with 12.2 mg of tetrabutylammonium acrylate. The reactor wassealed and heated to 100° C. In a 50 mL stainless vessel, 25 g ofbeta-propiolactone was added under nitrogen. The vessel was sealed andconnected to the reactor. Into the reactor containing tetrabutylammoniumacrylate, beta-propiolactone was injected with 50 psi of CO pressure at100° C. The reaction was agitated to 500 rpm, and monitored by in-lineIR. The plot of beta-propionate peak at 1836 cm⁻¹ andpoly(propiolactone) peak at 1739 cm⁻¹ as a function of time is shown inFIG. 21. After the temperature was stabilized, the reaction temperaturewas set to 140° C. At 36 min after the bPL addition, the reactionreached around 89% conversion, and 25 mL of water was added with 100 psiof CO at 140° C. After hydrolyzing the remaining beta-propiolactone, thepolymer was extracted with CH₂Cl₂. Volatiles were removed using arotovap and high vacuum to yield 17.7 g of a white solid. The solid wasanalyzed by ¹H NMR, TGA and melt rheology.

Example 2

Polymerization Production Using Plug-Flow Reactor Arrangement

A plug-flow reactor, consisting of two jacketed static mixers of ½″OD×24¾″ length and ˜60 mL volume, an 3-way nitrogen/feed inletball-valve and an outlet with a jacketed viscometer (Cambridge ViscosityViscoPro 2000 with 372 sensor), type K thermocouple, ATIR IR probe(Mettler-Toledo DS AgX Comp™ and ReactIR™ 15) and a 0-250 psigback-pressure regulator, was heated to 140° C. and purged with nitrogenat ambient pressure. A feed mixture was prepared by combining 0.1670 gof sodium acrylate (milled, sieved to 100 mesh and dried at 130° C.under vacuum, 0.001776 mol), 0.1536 g phenothiazine and 670 mL of□-propiolactone (˜760 g, 10.6 mol, chilled to −20° C.) in a one liter,pressure/vacuum rated GL45 bottle equipped with a magnetic stir-bar in aglove-box. The bottle was closed with a three port GL45 cap equippedwith a dip-tube and 2-way, ⅛″ ball-valve on one port, a ⅛″ 2-way-ballvalve with a 1 psi cracking-pressure check-valve on the second port anda ⅛″ 3-way ball-valve with one Luer-Lock fitting on the third port. Themixture was stirred briefly to dissolve the phenothiazine and suspendthe sodium acrylate. The sealed bottle was removed from the glove-box,transported to the plug-flow reactor, immersed in a water/ice bath ontop of a magnetic stirrer and connected via the three ⅛″ compressionfittings to a feed pump, a vent line (to a scrubber filled with 2%sulfuric acid) and a nitrogen needle-valve, respectively. The mixturewas stirred at 400 rpm to keep the sodium acrylate suspended. The 2-wayvent-valve was opened followed by switching the 3-way nitrogen/fillvalve from closed to nitrogen and adjusting the nitrogen needle-valve togive a steady stream of bubbles in the scrubber. The feed valve was thenopened followed by a prime valve on the feed pump (Eldex Optos 2SM,0.01-10.00 mL/min) and the pump was turned on at a flow rate of 5.00mL/min and allowed to run until the (Teflon FEP) line from the primeport to the scrubber showed that all bubbles had been ejected. The pumpwas then turned off, flow set to 0.50 mL/min, prime/feed 3-wayball-valve switched to feed, the reactor inlet 3-way ball-valve switchedfrom nitrogen to feed and the pump turned back on.

After 4 hours, the reactor exit back-pressure regulator was adjustedfrom ambient pressure to 200 psig and both the viscometer and theReactIR were turned on. After another hour and a half, the reactor wasfully pressurized, the viscometer (70 cP, compensated to 120° C.) andReactIR (˜95% conversion) readings were steady and product was collectedinto a one liter collection bottle which contained 300 mL ofmagnetically stirred water. After a further 22.5 hours, the feed mixturewas nearly exhausted and a 20 mL portion of chloroform was added to thefeed bottle via syringe and the Luer-Lock fitting on the nitrogen/fill3-way ball-valve. When the feed bottle was nearly empty again, another20 mL of chloroform was added. When that charge had been consumed, afurther 500 mL of chloroform was added. A fresh receiving bottle wasplaced on the reactor exit and conditions maintained for another 21hours when feed pump and circulating bath were turned off.

The crude product mixture from the first receiver bottle was transferredto a large blender with an additional 500 mL of water, blended until noparticles >5 mm were observed and the solid collected by filtration,air-dried and then vacuum dried at 40° C. for 20 hours to give 562.1grams of solid PPL product. The mixture of PPL solution in chloroformand aqueous liquid from the second receiver bottle was separated, thechloroform phase washed with water, dried and concentrated to 300 mL byazeotropic distillation and diluted in 600 mL of 2-propanol. Theresulting precipitate was collected by filtration, air dried and thendried in vacuo at 40° C. for 2 hours to give 90.5 grams of colorlesssolid PPL product. The filtrate was stripped of volatiles on a rotaryevaporator at 50° C. to give 45.0 g of clear, colorless oil, whichseparated into liquid and solid upon cooling.

1H NMR analysis suggested that solid from the first receiver wascomposed of 556 grams of PPL, with a molecular weight of ˜1210 g/molwith small amount (6 grams) of 3-hydroxypropionic acid (3-HPA) resultedfrom the hydrolysis of bPL in water (the GPC results showed Mn=275,Mw=1530 and Mn/Mw=5.56). The isolated solid from the second receivercontained 90 grams of PPL with a molecular weight of 2030 g/mol (the GPCresults showed Mn=328, Mw=1900, Mw/Mn=5.79) and 0.5 grams of 3-HPA.

POLYMERIZATION EXAMPLES Example 4 Batch Thermolysis of PPL to AcrylicAcid

A lab-scale batch thermolysis system consisting of a two-neckedround-bottom glass flask of 25 mL approximate internal volume (thereaction flask) was carried out. The reaction flask was equipped with aninternal thermocouple and the top center opening in the flask wasequipped with a short-path distillation apparatus. The short-pathdistillation apparatus consisted of a short path still (similar to AceGlass item #6554-06) with an additional thermocouple to monitor vaportemperature, followed by a water-cooled condenser, and finally afour-armed “cow” product receiver in a dry ice/acetone-cooled dewar. Thereaction flask was set in a fabric heating mantle, the power to whichwas controlled by a temperature controller that receives feedback fromthe thermocouple inside the reaction flask. Additional heat was providedwith electric heat tape, wrapped around the top of the reaction flaskand the distillation apparatus. The top of the reaction flask and thebottom of the distillation apparatus were insulated. The fabric heatingmantle was set above a magnetic stir plate, and a PTFE-coated stir barwas added to the reaction flask.

The tared reaction flask was charged with 90 mg dry sodium acrylate, 5mg PTZ, and 4.995 g of PPL produced from ring-opening polymerization ofsolvent-free bPL in the presence of sodium acrylate (at a concentrationof 1 mol per 6,000 mol of bPL) and phenothiazine (at a concentration of200 ppmw in bPL). In addition, the tared product receiver waspre-charged with 5 mg PTZ (distributed among the four product arms).After system assembly, the product receiver was attached to a nitrogenand vacuum source, and the air was displaced with nitrogen. Next, thereactor contents were heated to 90 deg C. to melt and begin stirring.The system was brought under vacuum to an absolute pressure ofapproximately 700 torr, and the reactor temperature setpoint was set to210 deg C. Internal reflux was observed inside the reaction flask withinminutes. It took 8-10 minutes to heat reactor contents up to 210 deg C.The moment the reactor contents reached 210 deg C. is defined as t=0.The reactor contents were held at 210 deg C. for 10 minutes, at whichpoint the reactor flask was mostly empty, save for a glassy darker solidand the stir bar.

It was later determined that the residual material in the reaction flaskweighed 156 mg. Four product samples were obtained—sample 129-098Acontained material collected until t=2 minutes, 129-098B containedmaterial collected between t=2 minutes and t=8 minutes, 129-098Ccontained material between t=8 minutes and t=9 minutes, and 129-098Dcontained collected material between t=9 minutes and t=10 minutes, whenheat sources were shut off. The total product collected weighed 4.7816g. Next, each sample was pipetted from the cow to labeled vials, andsamples were taken for 1H NMR (see FIGS. 25-28). NMR analysis suggestsan average acrylic acid content in 129-098A of 94.4%, in 129-098B of90.7%, in 129-098C of 90.6%, and in 129-098D of 92.5% by mass. Thebalance consists of di-acrylic acid ester and traces of other PPLoligomers where n>2.

POLYMERIZATION EXAMPLES Example 5 Batch Thermolysis of PPL to AcrylicAcid

A lab-scale batch thermolysis system consisting of a two-neckedround-bottom glass flask of 50 mL approximate internal volume (thereaction flask). The reaction flask was equipped with an internalthermocouple and the top center opening in the flask is equipped with adistillation apparatus. The distillation apparatus consisted of twoVigreux columns in series oriented coaxially (each similar to Ace Glassitem #6578-04), followed by an adapter with an additional thermocoupleto monitor vapor temperature, followed by a water-cooled condenser, andfinally a 50 mL round-bottom product receiver in a dryice/acetone-cooled dewar. The reaction flask was set in a fabric heatingmantle, the power to which is controlled by a temperature controllerthat receives feedback from the thermocouple inside the reaction flask.Additional heat was provided with electric heat tape, wrapped around thetop of the reaction flask and the distillation apparatus. The top of thereaction flask and the bottom of the distillation apparatus areinsulated. The fabric heating mantle was set above a magnetic stirplate, and a PTFE-coated stir bar is added to the reaction flask.

The tared reaction flask was charged with 1000 mg dry sodium acrylate,20 mg PTZ, and 19.162 g of PPL produced from ring-opening polymerizationof solvent-free bPL in the presence of sodium acrylate (at aconcentration of 1 mol per 6,000 mol of bPL) and phenothiazine (at aconcentration of 200 ppmw in bPL). In addition, the tared productreceiver was pre-charged with 5 mg PTZ. After system assembly, theproduct receiver was attached to a nitrogen and vacuum source, and theair was displaced with nitrogen. Next, the reactor contents were heatedto 90 deg C. to melt and begin stirring. The system was brought undervacuum to an absolute pressure of approximately 90 torr, and the reactortemperature setpoint was set to 165 deg C. Internal reflux was observedinside the reaction flask within minutes. It took approximately 10minutes to heat reactor contents up to 165 deg C. The moment the reactorcontents reached 165 deg C. is defined as t=0. The reactor contents wereheld at 165 deg C. for 40 minutes, at which point the reactor flask wasstill easily mixed by the stir bar.

It was later determined the residual material in the reaction flaskweighed 4.7186 g. Product sample 129-108 consisted of all collectedproduct, and weighed 14.6586 g. Next, a sample was taken for 1H NMR (seeFIG. 29). NMR analysis suggests an average acrylic acid content in129-108_Dist of 99.7%. The balance consists of di-acrylic acid ester andtraces of other PPL oligomers where n>2.

This application discloses several numerical ranges in the text andfigures. The numerical ranges disclosed inherently support any range orvalue within the disclosed numerical ranges even though a precise rangelimitation is not stated verbatim in the specification because thisinvention can be practiced throughout the disclosed numerical ranges.

The above description is presented to enable a person skilled in the artto make and use the invention, and is provided in the context of aparticular application and its requirements. Various modifications tothe preferred embodiments will be readily apparent to those skilled inthe art, and the generic principles defined herein may be applied toother embodiments and applications without departing from the spirit andscope of the invention. Thus, systems and methods described herein arenot intended to be limited to the embodiments shown, but are to beaccorded the widest scope consistent with the principles and featuresdisclosed herein. Finally, the entire disclosure of the patents andpublications referred in this application are hereby incorporated hereinby reference.

What is claimed is:
 1. A composition comprising: polypropiolactonehaving a concentration of greater than at least 90 wt %; a residualcobalt or ions thereof from a carbonylation catalyst in an amount of 10ppm or less; acetic acid in an amount of 10 ppm or less; andtetrahydrofuran in amount of 10 ppm or less.
 2. The composition of claim1, wherein the concentration of the polypropiolactone is greater than 95wt %.
 3. The composition of claim 1, wherein the polypropiolactonehaving a purity of at least 98 wt %.
 4. The composition of claim 1,wherein the composition comprises aluminum or ions thereof in an amountof 10 ppm or less.
 5. The composition of claim 1, wherein thepolypropiolactone has a number average molecular weight between 800g/mol and 100,000 g/mol and includes at least 95 wt % ofpolypropiolactone.
 6. The composition of claim 1, wherein at least 90%of polymer chains in the polypropiolactone have an acrylate end group.7. The composition of claim 1 wherein at least 90% of thepolypropiolactone have a formula of:

wherein Y is either —H or a cation and n is an integer from about 10 toabout 1,000.
 8. The composition of claim 1, wherein thepolypropiolactone has a polydispersity index of less than
 8. 9. Thecomposition of claim 1, further comprising β-propiolactone.
 10. Thecomposition of claim 1, wherein the composition includes cobalt or ionsthereof in an amount of less than 1 ppm.
 11. A composition comprising:polypropiolactone having a concentration of greater than at least 95 wt%; a residual cobalt or ions thereof from a carbonylation catalyst in anamount of 10 ppm or less; aluminum in an amount of 10 ppm or less; andtetrahydrofuran in amount of 10 ppm or less.
 12. The composition ofclaim 11, wherein the polypropiolactone having a purity of at least 98wt %.
 13. The composition of claim 11, wherein the composition has lessthan 10 ppm acetic acid.
 14. The composition of claim 11, wherein thecobalt or ions thereof are present in an amount of 100 ppb or less. 15.The composition of claim 14, wherein the aluminum is present in anamount of 100 ppb or less.
 16. The composition of claim 15, wherein thecomposition includes a beta-propiolactone level of 500 ppm or less. 17.The composition of claim 11, wherein the composition includes abeta-propiolactone level of 10 ppm or less.
 18. The composition of claim11, wherein the composition has a water content of 100 ppm or less. 19.The composition of claim 16, wherein the composition has a water contentof 50 ppm or less.
 20. The composition of claim 11, wherein thecarbonylation compound includes a porphyrin compound, a salen compound,or both